Inhibition of microtubule protrusion in cancer cells

ABSTRACT

The present invention generally concerns microtubule protrusions in cancer cells, including detached cancer cells, and inhibition of the protrusions. In particular aspects, the inhibition of the protrusions interferes with attachment of the cell to a vessel wall, and in further aspects the cell is killed by forcing it to enter capillaries and be destroyed, for example by shearing. Inhibition by a variety of agents and methods is contemplated.

The present invention claims priority to U.S. Provisional Patent Application Ser. No. 60/780,468, filed Mar. 8, 2006, which is incorporated by reference herein in its entirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

The present invention was developed at least in part with funds from the National Cancer Institute Howard Temin Career Award (K01-CA096555-01A1) and from the Department of Defense, Breast Cancer Concept Award (BC045699). The United States Government may have rights in the invention.

FIELD OF THE INVENTION

The present invention generally concerns at least the fields of cell biology, molecular biology, cancer, and medicine. In particular aspects, the present invention concerns the field of cancer therapy and/or prevention.

BACKGROUND OF THE INVENTION

Breast tumor cells can disseminate prior to significant primary tumor growth and remain dormant in distant tissues for extended periods of time (Naumov, MacDonald et al. 2001; Naumov, MacDonald et al. 2002; Schmidt-Kittler, Ragg et al. 2003). Survival, invasion and reemergence of such disseminated cells are primary determinants of tumor recurrence and patient death (Chambers, Groom et al. 2002). Detachment of epithelial cells from the extracellular matrix of their organ of origin causes cell rounding that leads rapidly to apoptotic cell death, a principle which is thought to limit metastatic spread (Frisch and Francis 1994; Reed 2003). In mammary epithelial cells, we have shown that apoptotic resistance allows cells to survive rounding, but additional genetic mutations are required for active tumor growth (Martin and Leder 2001; Martin, Ridgeway et al. 2004; Pinkas, Martin et al. 2004). Resistance to apoptosis by overexpression of survival proteins, like Bcl-2, prevents cell death during dissemination, but cell cycle arrest can still occur through activation of p53 (Nikiforov, Hagen et al. 1996; Nikiforov, Kwek et al. 1997). In solid tumors like breast cancer, detached cells generally remain arrested and must adhere to extracellular matrix in distant tissues to reinitiate growth (Naumov, MacDonald et al. 2001; Naumov, MacDonald et al. 2002). So while apoptotic resistance can promote extended bloodborne survival, additional mechanisms are required for tumor cells to escape blood vessels and successfully colonize distant tissues. (Naumov, MacDonald et al. 2001).

In vivo microscopy recently demonstrated that bloodborne tumor cells depend on tubulin polymerization to attach to the walls of capillary blood vessels (Korb, Schluter et al. 2004). However, any specific role for microtubules in this process remains unclear. Surprisingly, this recent study also showed that inhibiting actin polymerization greatly increased binding of tumor cells to blood vessel walls, even though actin depolymerization inhibits the actin-based invadopodia and podosomes that are well-known to affect the invasion of adherent tumor cells (Korb, Schluter et al. 2004). Bloodborne tumor cells therefore attach to capillary vessel walls via a cytoskeletal mechanism that is distinct from that of adherent cells, and is currently not well-characterized.

Recent genomic studies indicate that breast tumor cells may disseminate prior to significant primary tumor growth and remain dormant in distant tissues for extended periods of time (Schmidt-Kittler et al., 2003). Detachment of epithelial cells from the extracellular matrix of their organ of origin leads rapidly to apoptotic cell death, a principle which is thought to limit metastatic spread (Valentijn et al., 2004; Reddig and Juliano, 2005; Frisch and Francis, 1994). In mammary epithelial cells, apoptotic resistance will promote the survival of detached cells, but additional genetic mutations are required for active tumor growth (Pinkas et al., 2004; Martin et al., 2004). Resistance to apoptosis by overexpression of survival proteins, like Bcl-2, prevents cell death during dissemination, but cell cycle arrest can still occur through activation of p53 (Nikiforov et al., 1996; Nikiforov et al., 1997). Since these cells would survive but fail to actively grow, apoptotic resistance is one possible determinant of tumor dormancy (Townson et al., 2003).

However, evidence is accumulating that resistance to apoptotic cell death does not necessarily prevent early stress responses from occurring in cells. The apoptotically-resistant MDA-MB-231 cell line responds to hypoxic environments with increased invasiveness and the upregulation of cell surface α6β4 integrin (Yoon et al., 2005). Lymphocytic cell lines that overexpress Bcl-2 still generate reactive oxygen species in response to TNF-α, even though the later events in cell death are prevented (Liu et al., 2005). It is therefore important to consider whether apoptotically-resistant cells will truly remain dormant during the challenges of metastasis, or if they persistently respond to the challenging environment even though they are under a reduced threat of death.

Detachment of many adherent cell types from the extracellular matrix results in apoptotic cell death that arises from disrupted cell shape (see Valentijn et al, 2004; Reddig and Juliano, 2005 for review). In attached cells, tension generated by attachment of actin microfilaments to focal adhesions is counteracted by expansion of cytoplasmic microtubules to stabilize cell shape in a process termed tensegrity (Ingber, 2002; Wang et al., 2001). Disruption of this balance either by affecting cell attachment sites or directly inhibiting cytoskeletal structure induces rapid cell death (Chen et al., 1997; Martin and Leder, 2001). In order to survive detachment, epithelial cells must either avoid apoptosis or quickly reattach to adopt an appropriate cell shape. While tumor cells often develop resistance to apoptotic cell death, this phenomenon is rare in untransformed cells (Reed, 1999).

The present invention provides a long-felt solution to treating cancer, for example by preventing or reducing metastasis by targeting particular microtubule-associated structures heretofore unknown in the art.

SUMMARY OF EMBODIMENTS OF THE INVENTION

The present invention is directed to a system, methods, and compositions that relate to cancer therapy. In particular, embodiments of the present invention concern therapy that is related to microtubule protrusions in cancer cells, including in metastatic cancer cells, for example. In general embodiments of the invention, metastasis is inhibited or at least reduced in part by inhibition of the microtubule protrusion, for example by inhibition of a cellular mechanism required for establishment of a distant tumor.

It is described herein that mammary epithelial cell lines generate long and dynamic microtubule-driven protrusions of the plasma membrane after detachment. We also determine that detachment produces rapid detyrosination of α-tubulin, and the concentration of detyrosinated tubulin in protrusions. Full length α-tubulin contains a tyrosine residue at its c-terminus, and is termed Tyr-tubulin. Cleavage of this c-terminal tyrosine by a tubulin carboxypeptidase exposes a glutamic acid residue, yielding a detyrosinated form (Glu-tubulin) (Argarana, Arce et al. 1977; Argarana, Barra et al. 1978). Although this α-tubulin modification has been appreciated for thirty years, the identity of the gene encoding tubulin carboxypeptidase remains unknown. Glu-tubulin is post-translationally converted back to Tyr-tubulin, by a tubulin tyrosine ligase (TTL), which has recently been cloned in mice and humans (Erck, MacLeod et al. 2003). While microtubules containing Tyr-tubulin have a relatively short half-life, measured in minutes, Glu-tubulin is enriched in a more stable subset of microtubules (Webster, Gundersen et al. 1987). Microtubules containing Glu-tubulin can persist for hours and have been observed to remain for as long as 16 hours in nondividing cells (Webster, Gundersen et al. 1987). In breast tumor samples, increased levels of Glu-tubulin are associated with poor patient prognosis and an increased risk of cancer-related complications, but the mechanism for this effect is still unknown (Mialhe, Lafanechere et al. 2001).

The present invention relates to microtubule-based protrusions that promote reattachment of mammary epithelial cells to surfaces and each other, and may therefore allow detached cells to escape apoptosis by reattaching. Since this response persists in cells overexpressing Bcl-2 or Bcl-xL, it may promote the dormant dissemination of apoptotically-resistant tumor cells, even though they would not reinitiate growth until a much later time. Our data indicate that these microtubule protrusions do not necessarily originate from a tumor-specific mutation, since they are also observed in nontumorigenic mammary epithelial cell lines of both human and mouse origin. However, the persistence of this inherent microtubule response in apoptotically-resistant cells could have important consequences for the ability of disseminated tumor cells to efficiently adhere to new sites. The increased levels of Glu-tubulin upon detachment and its concentration in plasma membrane protrusions provide novel mechanisms to initiate microtubule-based tumor cell adhesion in blood vessels, and may explain why increased levels of Glu-tubulin in breast tumors predict poor patient survival.

The present invention generally concerns the previously unknown phenomenon that detached tumor cells generate microtubule protrusions that increase their ability to reattach to each other and/or surfaces. Because tumor cells become detached during spread through the blood or lymphatics, the generation of these protrusions is important for the ability of the tumor cells to spread metastatically to distant tissues and/or organs, in specific embodiments of the invention. In additional embodiments, such microtubule protrusions act to enhance tumor cell adhesion to vessel walls and/or allow tumor cells to avoid being crushed by size-restriction in capillaries. These protrusions increase in number and size per cell in more metastatic breast tumor cell lines. Protrusions also occur with a significantly higher frequency in populations of breast tumor cells with greater metastatic potential. In particular, death of cancer patients is most often caused by metastatic spread of the primary tumor through the bloodstream. However, large tumor cells are efficiently killed by shearing when they are pushed through small-diameter capillaries by blood pressure. The microtubule protrusions, in specific embodiments, help metastatic tumor cells avoid death by adhering to vessel walls and/or bracing against them before the size of the capillary becomes limiting. Inhibition of the function of these microtubule protrusions and/or inhibition of their production, for example, allows metastatic tumor cells to have a greater opportunity to be efficiently killed, such as by shearing through capillary beds, for example. In specific embodiments, the invention focuses on the role of these microtubule protrusions in the trapping and survival of tumor cells in distant capillary beds during metastatic spread.

Thus, in particular aspects of the invention, these microtubule protrusions are inhibited by one or more agents to specifically reduce the metastatic spread of tumors and tumor cells therein. In particular embodiments, an agent is delivered to an individual having cancer cells with one or more of the protrusions or is delivered to an individual at high risk for or susceptible to or suspected of having cancer cells with one or more of the protrusions. The agent is delivered such that it associates with at least one protrusion and thereby inhibits the function of the protrusion, degrades the protrusion, inhibits the activity of the protrusion, promotes degradation (such as an agent that promotes, facilitates or enhances ATP hydrolysis, for example) and/or prevents the protrusion from extending in length, for example. In alternative embodiments, the agent is delivered such that it associates with the cell and thereby inhibits the function of the protrusion, degrades the protrusion, inhibits the activity of the protrusion, promotes the degradation (such as an agent that facilitates or enhances ATP hydrolysis), and/or prevents the protrusion from extending in length. In additional or alternative embodiments, the agent may prevent the protrusion from being produced and/or prevent the protrusion from protruding (which may be referred to as extending) from the cell. The protrusion may be affected prior to extending from the cell, subsequent to extending from the cell, or is effective in either case. In certain aspects, the agent is selectively cytotoxic to detached cells, and in particular embodiments the agent kills apoptotic-resistant cells.

In embodiments of the invention, one or more components of a microtubule protrusion are inhibited, directly or indirectly. In particular aspects of the invention, the components comprise Glu-tubulin, kinesin and/or vimentin. Therefore, in specific embodiments of methods of the invention, one targets Glu-tubulin, kinesin and/or vimentin to inhibit one or more microtubule protrusions, for example from a cancer cell. In certain embodiments, the protrusions may be targeted by inhibiting Glu-tubulin, such as by one or more of the following, for example: 1) increasing activity and/or expression of tubulin tyrosine ligase (TTL), which postranslationally converts Glu-tubulin back to Tyr-tubulin; 2) inhibition of a carboxypeptidase that produces Glu-tubulin from Tyr-tubulin, such as by delivery of okadaic acid, 3-nitrotyrosine, 1-nor-okadone, Cantharidin, Phoslactomycin B (Fostriecin), DL-benzylsuccinic acid, Sodium orthovanadate, or a combination thereof, and in specific embodiments the carboxypeptidase is hAGBL3 (Rodriguez de la Vega et al., 2007). In certain embodiments, the protrusions may be targeted by inhibiting vimentin, such as by one or more of the following, for example: a dominant negative mutant, such as R113C and/or ΔC2B mutants; antisense or siRNA; and/or calyculin-A. In other embodiments, the protrusions may be targeted by inhibiting kinesin, such as by one or more of the following, for example: siRNA, including KIF5b siRNA, for example, lidocaine, and/or tetracaine.

In addition to, or alternative to, embodiments wherein one or more structural components of the microtubule protrusions are targeted, a regulatory molecule may be targeted that affects indirectly or directly the structural content of the microtubules. In specific cases, GSK-3b is not a structural component of microtubule protrusion, but a regulatory molecule. By phosphorylating APC and preventing it from binding microtubules, GSK-3b promotes microtentacle formation, in certain embodiments, but would not be a structural component (like Glu-tubulin, vimentin or kinesin).

In particular aspects, APC is a structural component, for example one that restricts microtubule protrusion extension. In specific embodiments, an agent is employed that enhances function of APC, such as, for example, lysophosphatidic acid (LPA) that can enhance the ability of APC to capture microtubules (Wen et al., 2004); and/or inhibition of GSK-3b, which enhances the function of APC by preventing phosphorylation.

In particular aspects of the invention, one or more methods of the invention employ inhibitors of one or more components of the microtubule protrusions and/or inhibitors of regulatory molecules and/or agents that enhance reduction of microtubule protrusions, and such compounds are delivered to the individual before and/or during and/or after surgery to prevent escape of residual cells during the wound healing that follows surgery. In particular embodiments, reduction of these microtentacles prevents tumor cells from successfully navigating the bloodstream. This could occur by preventing any attachment to the blood vessel wall (keeping the cells from invading distant tissues) or by causing them to fragment when passing through capillaries, for example.

Thus, as described above, in certain aspects of the invention, detyrosinated microtubule protrusions in detached cells promote reattachment. In fact, it is determined by the inventors that nontumorigenic mammary epithelial cell lines generate long and dynamic microtubule-driven protrusions of the plasma membrane in response to detachment. These protrusions promote reattachment of cells to surfaces and each other, and may therefore allow detached cells to escape apoptosis. Since this response persists in cells overexpressing Bcl-2 or Bcl-xL, it indicates that disseminated apoptotically-resistant cells are not as dormant as previously suspected. The data indicate that these microtubule protrusions do not necessarily originate from a tumor-specific mutation, but nevertheless have important consequences for the ability of tumor cells to efficiently adhere to new sites, in certain embodiments of the invention.

Time-lapse video microscopy of detached mammary epithelial cells detected the extension of long, dynamic protrusions of the plasma membrane, and the present inventors have characterized the cytoskeletal mechanism underlying this novel observation. Nontumorigenic mammary epithelial cell lines of both human and mouse origin produce such protrusions, indicating that it is likely an inherent characteristic of the untransformed cells. This response may be relatively short-lived, in specific embodiments, since mammary epithelial cells die by apoptosis within about 24 hours in suspension. However, cell lines that resist apoptosis through expression of either Bcl-2 or Bcl-xL will persistently form protrusions. Previous studies by the inventors indicate that such apoptotically-resistant cell lines will not form tumors in mice and lie dormant in distant tissues, in specific embodiments of the invention. Given the persistent motility response in these detached cells, they may not be as dormant as previously suggested. These protrusions can be inhibited with tubulin-depolymerizing agents such as colchicine, colcemid, vinblastine, vincristine, nocodazole and myoseverin, for example, but are enhanced by the actin-depolymerizing agent, Latrunculin-A or Cytochalasin-D. Immunofluorescence microscopy and Western blotting demonstrate that the protrusions are largely comprised of detyrosinated Glu-tubulin, a post-translationally modified form of tubulin that is found in stabilized microtubules. These microtubule processes can extend more than 3 times the cell diameter, and undergo a rapid probing motion more than once per second. Formation of these microtubule protrusions is necessary for efficient cell-cell and cell-substratum attachment. In particular embodiments of the invention, this inherent microtubule response in detached mammary epithelial cells provides at least some of the invasive characteristics of breast cancer, independent of any tumor-specific genetic alteration, for example.

In particular embodiments of the invention, a diagnostic application is employed. In certain aspects of the invention, the identification of one or more cells with microtubule protrusions is indicative of the presence of cancer, for example metastatic cancer. In fact, given that a higher incidence of protrusions is present in highly metastatic tumor cells, in specific embodiments this serves as a diagnostic test. In a specific embodiment, a sample is obtained from an individual at high risk for developing cancer, suspected of having cancer, known to have cancer, or at high risk for developing metastatic cancer, known to have metastatic cancer, or suspected of having metastatic cancer, for example. The sample is assayed for the presence of one or more protrusions on one or more cells.

The assay to detect cells with protrusions may comprise any suitable method and reagents to identify the presence of one or more protrusions, and in specific embodiments the assay comprises identifying distinguishing cell morphology. In additional embodiments, one or more cells may be assayed for the presence of one or more gene products particularly associated with the protrusions, such as the compositions thereof, including polypeptides, for example. In further embodiments, the expression of a polynucleotide encoding one or more gene products particularly associated with the compositions of the protrusions may be assayed. Thus, in specific embodiments the assay utilizes reagents such as nucleic acid, polypeptide, antibodies, small molecules, mixtures, combinations, and so forth. In specific embodiments, compositions such as RNA or DNA viruses are employed, such as for viral gene therapy, for example. Samples of any suitable kind may be obtained from the individual to assay for protrusions, although in specific embodiments the samples comprise blood; plasma; serum; tissue, including vessel tissue; bone; bone marrow; and so forth.

In other embodiments of the invention, there are methods and reagents for preventing cancer, including preventing metastatic cancer, for example. In particular aspects, the term “preventing” encompasses prevention from occurrence, delay of onset, reduction in intensity, reduction in prevalence, and/or reduction in recurrence, for example. In specific aspects of the invention, one or more agents of the invention are administered to an individual not known to have metastatic cancer, including one suspected of having cancer or one susceptible for developing cancer, including metastatic cancer. In certain cases, an agent of the invention is provided to an individual upon or soon after diagnosis of the cancer to prevent metastasis. In one exemplary embodiment, an individual with a primary tumor receives the agent of the invention before and/or at the time of surgery and/or treatment of the primary tumor, although in alternative embodiments the individual receives the agent of the invention subsequent to the time of surgery and/or other treatment of the primary tumor, or the individual receives the agent at both times. In animal models, surgery or photodynamic therapy of primary prostate tumors have been shown to actually increase the incidence of lung metastasis (since damage to the primary tumor induces wound healing, blood vessel growth, etc., that provides an opportunity for any surviving cells to escape the primary site) (Momma et al., 1998). Thus, in certain embodiments of the invention, an individual is treated with an inhibitor of protrusions at the time of and/or prior to surgery or treatment so that any escaping cells would be more likely to be shredded in distant capillary beds.

Epithelial cells are important for biological barriers, in certain instances, for example, in skin and lung lining. Thus, in specific embodiments of the invention, the cancer cells related to the invention are epithelial cells and once they are circulating they are biologically driven to establish a barrier or become part of an existing barrier. More than 90% of human solid tumors arise as carcinomas from epithelial cells (Birchmeier, 1996), so how epithelial cells respond to detachment is relevant to the treatment of human cancers, in particular embodiments. Therefore, the epithelial cell employs a mechanism to search for other cells to include in a barrier, and in specific embodiments of the invention the microtubule protrusions are employed by the cell to establish a barrier or incorporate the cell into an existing barrier. In specific embodiments, the microtubule protrusions move to search for other cells to form the barrier, yet once they contact another cell, those protrusions then remain stationary on the contacted cell, at least temporarily.

In some aspects of the invention, cancer cells enter the bloodstream and become destroyed by pressure from the size of the capillary beds unless the cell can prevent reaching the capillary beds, yet this event is difficult to measure because it occurs rapidly. However, in certain embodiments of the invention, a signal associated with the cell, such as luciferase on a vector or genome in the cell, signifies the location of the cell and, if applicable, its subsequent destruction. For example, cancer cells that harbor luciferase are delivered to mice, luciferin substrate is delivered to the mice, and subsequent tracking of the signaling cells can be employed. The inventors demonstrate that when cancer cells with a high number of microtubule protrusions are injected into mice, one can observe them localizing within minutes to the lungs. In specific embodiments, luciferase cancer cells with lower numbers of microtubules push through the capillaries and retention in the lungs would be reduced. If tumor cells are treated with drugs that inhibit the microtubule protrusions before and/or during and/or after injection of the cells into the mice, then in certain embodiments fewer cells remain in the lungs and more tumor cells become fragmented by forced passage through narrow lung capillaries. The destruction of cells in the capillary beds may be observed by looking for cell fragments in blood downstream of the lung, for example. In embodiments wherein visualization of cells is desired, one may employ a signal that lasts longer than standard fluorescence, such as quantum dot, which utilizes fluorescence that essentially never fades.

In certain embodiments of the invention, the outer surface of cancer cells, such as tumor cells, is more flexible than a normal cell, and therefore the microtubule protrusions more easily protrude from the cell. In specific embodiments, this is the result of a weaker actin cortex in a cancer cell, and Glu-tubulin may be sufficient to sustain the protrusion, for example without vimentin and kinesin or considerably reduced levels of vimentin and kinesin. In these cases, it is preferable to target Glu-tubulin over vimentin and/or kinesin, although vimentin and/or kinesin may be targeted in addition to Glu-tubulin.

In particular aspects of the invention, a cancer cell is further defined as a detached cancer cell, and it may be from breast, prostate, pancreatic, colon, lung, brain, liver, ovarian, testicular, cervical, gall bladder, spleen, bone marrow, head and neck, stomach, kidney, or bone bladder, skin, oral, throat, esophageal, thyroid cancer, for example. In further specific embodiments, the individual has metastatic cancer, is suspected of having metastatic cancer, or is susceptible to metastatic cancer. In specific embodiments, the cell is an epithelial cancer, such as a carcinoma.

In an additional embodiment of the present invention, there is a method of preventing metastasis of cancer in an individual, comprising the step of administering to the individual one or more agents that target one or more microtubule protrusions from at least one cancer cell in the individual.

In another embodiment, there is a pharmaceutical composition comprising an agent that targets at least one component of a microtubule protrusion from a cell, and a pharmaceutically acceptable carrier.

In an additional embodiment, there is a kit comprising an agent that targets at least one component of a microtubule protrusion from a cell, wherein said kit is housed in a suitable container.

In another embodiment, there is a method of screening for an agent that targets at least one component of a microtubule protrusion from a cell, comprising the steps of: providing a microtubule protrusion from a cell or a component of the protrusion; and providing a candidate modulator, wherein when the candidate modulator associates with one or more components of the microtubule protrusion, said candidate modulator is the agent. The candidate modulator may be a small molecule, a nucleic acid, a polypeptide, a peptide, an antibody, or a mixture or combination thereof, for example. The method may occur in vitro or in vivo. In specific embodiments, the method further comprises manufacturing of the agent. In other specific embodiments, the agent is delivered to an individual with cancer, an individual at high risk or suspected of having cancer, or an individual susceptible to having metastatic cancer, for example.

In certain embodiments, the present invention provides that detyrosinated microtubule protrusions in suspended mammary epithelial cells promote reattachment.

The skilled artisan recognizes that while observations related to the invention are in breast tumor cell lines, this principle could be therapeutic for many different cancer types. Examples of other cancers for which the invention may be utilized include at least prostate, pancreatic, colon, lung, brain, liver, ovarian, testicular, cervical, gall bladder, spleen, bone marrow, head and neck, stomach, kidney, bone, bladder, skin, oral, throat, esophageal, thyroid and so forth. In particular aspects of the invention, the cancer is resistant to one or more cancer therapies, such as tamoxifen, cisplatin, bortezomib, doxorubicin, paclitaxel, letrozole, trastuzumab, vinblastine, raloxifene hydrochloride, irinotecan, gefitinib, fulvestrant, and so forth.

In an additional embodiment of the invention, there is a method of reducing the risk of a tumor cell from a first organ in an individual to establish a malignancy in a second organ in the individual, comprising delivering a therapeutically effective amount of an agent that targets one or more microtubule protrusions of the tumor cell. In a specific embodiment, the tumor cell releases from the tumor upon therapy for the tumor, such as upon surgery in the individual, for example. Releasing of the tumor cell from a primary tumor mass may be caused directly or indirectly upon utilizing the therapy. In further embodiments, the method may be further defined as the tumor cell releasing from the tumor upon excision of the tumor from the individual. In specific aspects, the tumor cell is released from a primary tumor mass during excision of at least part of the primary tumor mass from the individual. Therefore, in particular aspects this clarifies the difference between the primary tumor mass and the residual tumor cells left in the body (which would be at risk of spreading metastatically to distant tissues during wound healing). In particular cases, the method is further defined as the tumor cell releasing from the primary tumor mass during removal of the primary tumor mass from the individual and/or during therapy for the primary tumor mass for the individual. In other cases, the method is further defined as the tumor cell being one that remains in the body of the individual during removal of a primary tumor mass from the individual and/or during therapy for the primary tumor mass for the individual. In additional embodiments, the agent is delivered to the individual before, during, and/or after the surgery.

The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter which form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and specific embodiment disclosed may be readily utilized as a basis for modifying or designing other structures for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent constructions do not depart from the spirit and scope of the invention as set forth in the appended claims. The novel features that are believed to be characteristic of the invention, both as to its organization and method of operation, together with further objects and advantages will be better understood from the following description when considered in connection with the accompanying figures. It is to be expressly understood, however, that each of the figures is provided for the purpose of illustration and description only and is not intended as a definition of the limits of the present invention.

DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the present invention, reference is now made to the following descriptions taken in conjunction with the accompanying drawings.

FIGS. 1A-1C show that detachment induces cellular protrusions in both normal and Bcl2-expressing mammary epithelial cells. In FIG. 1A, human MCF10A or mouse EpH4 mammary epithelial cell lines produce protrusions of the plasma membrane when plated over agarose and photographed live (black arrows). Apoptosis becomes apparent in detached MCF10A and EpH4 cells after 24 hours of detachment and almost all cells are dead by 48 hours, as indicated by darkening and condensation of the cells. EpH4 cells that overexpress Bcl-2 (EpH4-Bcl2) remain largely viable at 48 hours and continue to produce protrusions. In FIG. 1B, EpH4 cells or those overexpressing Bcl-2 were placed in suspension for the indicated time in hours. Cleavage of PARP to a truncated form (ΔPARP), indicates that apoptosis is largely complete in EpH4 cells after 16 hours, while relatively few EpH4-Bcl2 cells die even after 24 hours. In FIG. 1C, EpH4 cells that produce protrusions (white arrows) continue to exclude propidium iodide, indicating an intact plasma membrane. Similar results were obtained with MCF10A cells.

FIGS. 2A-2B show that cytoskeletal inhibitors affect cellular protrusions. In FIG. 2A, after 15 minutes of suspension, protrusions in EpH4 and MCF10A cells are quite small (Control, white arrows). Treatment with the actin depolymerizing agent, Cytochalasin-D, increased protrusions (white arrowheads) and this effect was even more pronounced with the actin inhibitor Latrunculin-A (LA, 5 μM). The microtubule depolymerizing agent, Colchicine (1 μM) prevented protrusions. The combination of LA and Colchicine (LA+Col) prevented protrusion formation, and those that did form appeared to be fragmented (black arrow). In FIG. 2B, populations of live, suspended cells were scored blindly for two or more protrusions longer than the cell radius. Each bar represents the mean±S.D. for three experiments in which at least 100 single cells were counted.

FIG. 3 shows that protrusions are microtubule-based. EpH4 cells were suspended in either DMEM (Control) or media containing 5 μM Latrunculin-A (LA), 1 μM Colchicine or the combination of both drugs for 30 minutes. Cells were then spun onto glass coverslips and fluorescently stained for α-tubulin (green) and polymerized actin (red). Protrusions that are difficult to see by phase contrast are easily discernible with immunostaining for α-tubulin (white arrows). Protrusions contain little polymerized actin, except at points of concentration, which are often at the end (arrowhead). Depolymerization of actin with LA strongly enhances the formation of microtubule protrusions.

FIG. 4 demonstrates that protrusions are enriched in detyrosinated α-tubulin. EpH4-Bcl2 cells were grown on glass coverslips (Attached) or suspended over agarose for one hour in the presence of LA (5 μM) to enhance protrusion formation (Detached). Immunostaining for different posttranslationally-modified forms of tubulin indicates differential localization in attached and suspended cells. Full-length α-tubulin, Tyr-tubulin and Acetyl-tubulin localize predominantly to the cell body in detached cells rather than specifically along the extended protrusions visible by phase-contrast (black arrows). Detyrosinated α-tubulin (Glu-tubulin) is enriched in the protrusions relative to the cell body, and is also found in centrosomes (white arrows).

FIGS. 5A-5B show that cellular levels of Glu-tubulin increase in response to detachment. EpH4-Bcl2 cells were grown attached to tissue culture dishes or suspended over agarose for the indicated times in either the absence or presence of LA (5 μM). In FIG. 5A, cell lysates were immunoblotted to detect levels of modified tubulin isoforms in the cell populations. In FIG. 5B, modified α-tubulin isoforms were normalized to total α-tubulin and then compared relative to the levels in attached cells at time zero. Bars represent the mean±S.E.M. of four independent experiments. While Glu-tubulin increases significantly in response to detachment (P<0.05, t-test), none of the other tubulin forms increase significantly (P>0.05, t-test). Differences in Glu-tubulin upon detachment were also statistically-significant when compared to matched controls at time zero or one hour (black asterisks). LA treatment does not significantly increase cellular levels of Glu-tubulin in either attached or detached cells (P>0.05, t-test).

FIGS. 6A-6B demonstrates that microtubule protrusions are required for efficient cell attachment. In FIG. 6A, EpH4-Bcl2 cells were suspended over agarose and treated with inhibitors as above. Following treatment, cells were plated into 0.3% methylcellulose media over agarose and the rate of cell-cell attachment was followed by Hoescht DNA staining. While LA-treated cells cluster similarly or even more tightly compared to control cells after 5 hours (black arrow), cells treated with tubulin polymerization inhibitors are significantly delayed in clustering. Similar results were found in three independent experiments. In FIG. 6B, EpH4-Bcl2 cells suspended over agarose for one hour in DMEM or DMEM containing LA (5 μM), Colchicine (1 μM), or the combination. Reattachment of these cells to either uncoated tissue culture plates or those pre-coated with laminin was followed by XTT cell viability assay. Values represent mean±S.D. of raw XTT values of three separate experiments. While actin depolymerization with LA does not affect cell-surface attachment, depolymerization of tubulin with colchicine significantly prevents initial cell attachment to either uncoated or laminin-coated plates.

FIG. 7 demonstrates that metastatic breast tumor cell lines have more frequent and numerous protrusions.

FIG. 8 demonstrates that protrusions can be reduced by chemical inhibition of specific signaling proteins.

FIG. 9 illustrates how circulating tumor cells may become part of a metastatic tumor, in specific embodiments. In particular, circulating cells eventually get destroyed in the capillaries unless they adhere to the blood vessel walls.

FIG. 10 shows GFP-membrane expression provides high-contrast protrusion imaging.

FIG. 11 shows that microtubule protrusions mediate binding to adjacent cells. GFP labeling of protrusions allows them to be observed in cell clusters, where not all cells express GFP (white arrows).

FIG. 12 shows that GFP-membrane labeling identifies variations in protrusion frequency. GFP labeling of protrusions allows detection of protrusions that were previously not visible by phase-contrast microscopy. Bars represent mean±S.D. for three experiments in which the indicated breast tumor cell lines were transfected with GFP-membrane and at least 100 cells were scored blindly for protrusions.

FIG. 13 demonstrates that lower Glu-tubulin levels correlate with lower protrusion frequency. Western blotting for levels of Glu-tubulin shows that the SkBr3 cell line, which has the lowest protrusion counts also has the lowest levels of Glu-tubulin.

FIG. 14 demonstrates that increases in Glu-tubulin persist in apoptotically-resistant cells. Western blotting shows that Glu-tubulin levels increase in MCF10A cells during suspension, but begin to diminish by 16 hours. Glu-tubulin levels remain high in cells that overexpress Bcl-2 and resist apoptosis (10A-Bcl2).

FIG. 15 demonstrates that chemical inhibition of GSK-3β is not toxic to cells.

FIG. 16 shows that kinesin inhibition with local anesthetics reduces protrusions in breast tumor cells.

FIG. 17 demonstrates that lidocaine is not cytotoxic at higher concentrations and tetracaine is cytotoxic at higher concentrations.

FIG. 18 shows that local anesthetics do not induce apoptosis until after 6 hours of treatment. Cleavage of PARP protein indicates apoptosis.

FIG. 19 demonstrates that truncated APC expression (˜170 kDa) correlates with increased protrusions.

FIG. 20 shows inducible full-length (˜300 kDa) APC expression in exemplary HT-29 cells. Increased levels of ˜250 kDa form after induction may indicate that cleavage of full-length APC occurs.

FIG. 21 illustrates an exemplary strategy to provide and/or identify therapeutic targets in protrusions.

FIG. 22 shows bioluminescent imaging of transplanted tumor cells.

FIG. 23 shows imaging the trapping of circulating breast tumor cells in the lungs of living mice (15 minutes post injection into the tail vein).

FIG. 24 shows combined fluorescence/bioluminescence imaging (cell division-fragmentation).

FIG. 25 shows an exemplary structural schematic of a microtubule protrusion, wherein the protrusion is comprised of Glu-tubulin utilizing a kinesin-based mechanism for its interaction with vimentin.

FIG. 26 illustrates that at least some microprotrusions are enriched in Glu-tubulin and vimentin, in specific embodiments.

FIG. 27 demonstrates that numerous, thick protrusions correlate with high vimentin and low cytokeratin (***, Bt-474 and MDA-436), and that persistence of vimentin in suspension also correlates.

FIG. 28 shows that there are increased vimentin levels and stability in cell lines with high protrusions.

FIG. 29 shows that vimentin increases persist in apoptotically-resistant cells.

FIG. 30 shows that suspension increases vimentin levels, which persist in apoptotically-resistant cells.

FIG. 31 provides an exemplary vimentin blot for different cell lines, in the presence or absence of LA and suspended for one hour or not.

FIG. 32 demonstrates that transient expression of vimentin increases protrusions.

FIG. 33 illustrates an exemplary Hs578t/Bt474 timecourse for an exemplary vimentin siRNA, Vim4.

FIG. 34 shows siRNA knockdown of vimentin in exemplary human vimentin-expressing cell lines HS578t and Bt 474 over time.

FIG. 35 demonstrates that pretreatment with okadaic acid or calyculin-A reduces microtentacles.

FIG. 36 shows that vimentin can be efficiently downregulated with siRNA.

FIG. 37 provides demonstration of quantitation of siRNA-mediated vimentin downregulation.

FIGS. 38A-38C provide an exemplary schematic showing interaction of microtentacles with the actin cortex. Truncation of APC in tumor cells (ΔAPC) or its phosphorylation by GSK-3b allow microtubules to extend past the actin cortex to produce microtentacles. Inhibiting Src family kinases may reduce microtentacles by increasing crosslinking in the actin cortex.

DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION I. Definitions

In keeping with long-standing patent law convention, the words “a” and “an” when used in the present specification in concert with the word comprising, including the claims, denote “one or more.” Some embodiments of the invention may consist of or consist essentially of one or more elements, method steps, and/or methods of the invention. It is contemplated that any method or composition described herein can be implemented with respect to any other method or composition described herein.

The term “detached cancer cell” as used herein refers to a cancer cell, such as a tumor cell, that has escaped its primary organ site, and now is present elsewhere in the body of the patient, such as residing elsewhere in the body of the patient, for example. In specific embodiments, the detached cancer cell is in the bloodstream.

The term “detyrosinated Glu-tubulin” as used herein refers to α-tubulin in which the carboxyl-terminal tyrosine residue has been removed and now exposes a glutamic acid residue at its carboxyl-terminus.

The term “distant tumor” as used herein refers to a tumor cell that has separated from its organ of origin and now resides elsewhere in the body.

The term “microtubule protrusion” as used herein refers to extensions of the plasma membrane in detached cells that are enriched in tubulin protein, for example Glu-tubulin and largely devoid of polymerized actin. When treated with inhibitors of actin depolymerization, there is enhancement of the protrusions, such as with the protrusions increasing in length, number per cell and frequency in a population, for example. This is in contrast to well-known invadopodia and podosomes associated with adherent tumor cells that are actin-based and inhibited by actin depolymerization.

II. Embodiments of the Present Invention

Breast tumor cells enter the bloodstream long before the development of clinically evident metastasis. However, the early presence of such bloodborne cells predicts poor patient outcome. Nearly 90% of human breast tumors arise as carcinomas from mammary epithelial cells, so it is important to characterize how these cells respond to the detached conditions that they would experience in the bloodstream. In the present invention, mammary epithelial cell lines produce long and dynamic protrusions of the plasma membrane when detached. Although human and mouse mammary epithelial cell lines die by apoptosis within 16 hours of detachment, this protrusive response persists for days in cells overexpressing either Bcl-2 or Bcl-xL, for example. Unlike actin-dependent invadopodia and podosomes, these protrusions are actually enhanced by actin depolymerization with Cytochalasin-D or Latrunculin-A. Immunofluorescence and Western blotting demonstrate that the protrusions are enriched in detyrosinated Glu-tubulin, a posttranslationally modified form of α-tubulin that is found in stabilized microtubules. Video microscopy indicates that these protrusions promote cell-cell attachment, and inhibiting microtubule-based protrusions correlates with reduced extracellular matrix attachment. Since bloodborne metastasis depends on both cell-cell and cell-matrix attachment, microtubule-based protrusions in detached mammary epithelial cells provide a novel target that could influence the metastatic spread of breast tumors.

Thus, in specific aspects of the invention, there are methods and compositions associated with particular cancer cells that comprise one or more microtubule protrusions from the cell. In particular aspects of the invention, the microtubule protrusions are utilized by the cell to attach to an entity, such as a tissue, and including a blood vessel wall. Such attachment in certain aspects protects the cancer cell from the destruction caused by forcing it through a capillary vessel, and in additional aspects the attached cancer cell escapes through the vessel wall.

Thus, in some embodiments of the invention the microtubule protrusions are targeted to prevent attachment to a surface such as a blood vessel wall. In particular embodiments, an agent is delivered to an individual having cancer cells with one or more of the protrusions or is delivered to an individual susceptible to having cancer cells with one or more of the protrusions. The agent is delivered such that it associates with at least one protrusion and thereby inhibits the function of the protrusion, degrades the protrusion, inhibits the activity of the protrusion, promotes degradation (such as an agent that promotes, facilitates or enhances ATP hydrolysis) and/or prevents the protrusion from extending in length, for example. In alternative embodiments, the agent is delivered such that it associates with the cell and thereby inhibits the function of the protrusion, degrades the protrusion, inhibits the activity of the protrusion, promotes the degradation (such as an agent that facilitates or enhances ATP hydrolysis), and/or prevents the protrusion from extending in length. In additional or alternative embodiments, the agent may prevent the protrusion from being produced and/or prevent the protrusion from protruding (which may be referred to as extending) from the cell. The protrusion may be affected prior to extending from the cell, subsequent to extending from the cell, or is effective in either case. In certain aspects, the agent is selectively cytotoxic to detached cells, and in particular embodiments the agent kills apoptotic-resistant cells, for example.

Upon delivery of the agent to the individual, one or more protrusions from a cancer cell are affected, such as is described herein, and in particular embodiments the cell is a metastatic cancer cell, which in some cases is a detached cancer cell, such as from a tumor. In particular embodiments of the invention, metastatic cancer is prevented, is reduced in prevalence, is reduced in mass, or is delayed. In certain aspects of the invention, at least one symptom related to cancer is improved directly or indirectly because of the invention.

Cancer cells of the invention that may be targeted by methods and/or compositions of the invention may be of any suitable kind. In particular cases, the cancer cells are from a solid tumor. In specific aspects, the cancer cells are cells that are in a tumor, such as a primary tumor, for example, or that are released from a tumor, or that are left behind at a tumor site upon removal of at least part of the primary tumor mass. In specific embodiments, the tumor cells are not restricted to cells directly detaching from the primary tumor, but are residual cells remaining at the surgical or therapeutic site. Thus, the present invention not only kills cells that directly remain or escape during the procedure, but also cells that are missed entirely by the surgery or therapy. For example, increased metastasis due to wound healing can even be seen with localized therapies, such as photodynamic therapy, and does not have to be restricted to surgical approaches. The damage caused to local tissue by radiotherapy, photodynamic therapy, localized heating or other such approaches could free cells that could be destroyed by targeting microtubule protrusions. The tumor cells that evade therapy of any kind, including surgery, chemotherapy, immunotherapy, radiation, photodynamic therapy, and so forth, may be targets of the invention.

III. Therapeutic Agents of the Invention

In certain embodiments of the invention, an agent that targets microtubule protrusions is utilized to inhibit the function, activity, or production of the protrusion. Any suitable agent may be employed, although in specific aspects the agent comprises one or more small molecules; one or more polypeptides; one or more antibodies; one or more nucleic acids; including RNA, DNA; or a mixture or combination thereof, and so forth. In specific embodiments, RNA or DNA viruses are employed in the invention, such as for viral gene therapy, for example.

In particular embodiments, the agent affects the protrusion by inhibiting the function, activity, or synthesis of the protrusion, or by enhancing the degradation of the protrusion, for example. However, in some embodiments, the agent affects cells that are detached and at some point during the life of the cell comprised one or more protrusions.

In certain aspects, the agent of the invention comprises one or more inhibitors, and the inhibitors are administered to an individual in need thereof, such as an individual that has cancer, which may be metastatic cancer, in some embodiments, and the individual may be suspected to have metastatic cancer or may be susceptible to cancer including metastatic cancer, for example.

Although the agent may affect any composition of the microtubule protrusions directly or indirectly, exemplary targets are as follows.

A. Agents that Affect Detyrosinated Glu-Tubulin

In particular aspects of the invention, one or more agents that affect detyrosinated glu-tubulin (also referred to as alpha-tubulin, for example) is employed. In specific embodiments they comprise one or more inhibitors of detyrosinated glu-tubulin, although in alternative embodiments they comprise one or more agents that induce, initiate, or facilitate breakdown of the protrusions. Alpha-tubulin is detyrosinated by a yet unknown carboxypeptidase enzyme to form glu-tubulin. The counteracting enzyme, tubulin tyrosine ligase has been identified. The formation of detyrosinated glu-tubulin could be prevented by either inhibiting the action of the unknown carboxypeptidase, or by enhancing the activity of tubulin tyrosine ligase, or both, for example. Any inhibitor of detyrosinated glu-tubulin function or its synthesis may be employed, although in specific embodiments the inhibitor comprises an antibody; a small molecule compound; a hydrolyzable nucleotide triphosphate, such as ATP, GTP, and/or UTP, for example; one or more nucleic acids; including RNA, DNA; or a mixture or combination thereof, and so forth; or a mixture or combination thereof.

1. Inhibitors of Tubulin Carboxypeptidase

In certain embodiments of the invention, one or more inhibitors of tubulin carboxypeptidase are employed, such as the following: 1) 3-nitrotyrosine; 2) okadaic acid; 3) 1-nor-okadone; 4) cantharidin; 5) Phoslactomycin B (Fostriecin); 6) siRNA against hAGBL3; 7) chemical inhibitors specifically against hAGBL3 activity; 8) DL-benzylsuccinic acid; 9) Sodium orthovanadate, or combinations thereof.

2. Tubulin Depolymerizers

In certain embodiments of the invention, one or more depolymerizers of tubulin, such as one or more of the following: 1) Colchicine; 2) Vinblastine; 3) Vincristine; 4) Nocodazole; 5) Phomopsin A; 6) Vindesine; 7) Myoseverin; 8) Cytochalasin E; 9) Podophyllotoxin; 10) Etoposide; 11) Griseofulvin; or a combination thereof.

3. Tubulin Stabilizers

In certain embodiments of the invention, one or more stabilizers of tubulin are employed, such as to stop motion of the microtubule protrusions, such as one or more of the following: 1) Paclitaxel; 2) Docetaxel; 3) Epothilones, or a combination thereof.

B. Agents that Affect GSK-3

In particular aspects of the invention, one or more agents that affect GSK-3 is employed, and in specific aspects the one or more agents comprises an inhibitor of GSK-3. The inhibitor may act directly on GSK-3 or may act indirectly on another molecule that affects GSK-3. In some embodiments the compositions comprise one or more agents that induce, initiate, or facilitate breakdown of the protrusions. Any inhibitor of GSK-3 may be employed, although in specific embodiments the inhibitor comprises an antibody; agents such as those identified in U.S. Patent Publication No. US 2005/0026946, the entirety of which is incorporated by reference herein; C₁₆H₁₀BrN₃O₂ (GSK-3 Inhibitor IX (Cat. No. 361550; Calbiochem®, San Diego, Calif.); insulin, such as with lithium; SB-415286, such as with lithium (MacAulay et al., 2003; Coghlan et al., 2000); CT118637 (Dokken et al., 2005); GSK-3 Inhibitor 1—Calbiochem 361540; GSK-3 Inhibitor II—Calbiochem 361541; GSK-3 Peptide Inhibitor I—Calbiochem 361545; GSK-3 Peptide Inhibitor II—Calbiochem 361546; GSK-3 Inhibitor VII—Calbiochem 361548; GSK-3 Inhibitor VIII—Calbiochem 361549; GSK-3 Inhibitor XI—Calbiochem 361553; GSK-3 Inhibitor XII—Calbiochem 361554 and so forth.

In certain embodiments of the invention, one or more inhibitors of GSK-3b are employed, such as one or more of the following: 1) Lithium; 2) 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione; 3) 2-Thio(3-iodobenzyl)-5-(1-pyridyl)-[1,3,4]-oxadiazole; 4) 2,4-Dibenzyl-5-oxothiadiazolidine-3-thione; 5) 2-Chloro-1-(4,5-dibromo-thiophen-2-yl)-ethanone; 6) α-4-Dibromoacetophenone; 7) N-(4-Methoxybenzyl)-N′-(5-nitro-1,3-thiazol-2-yl)urea; 8) (2′Z,3′E)-6-Bromoindirubin-3′-oxime; 9) 3-(1-(3-Hydroxypropyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-4-pyrazin-2-yl-pyrrole-2,5-dione; 10) (5-Methyl-1H-pyrazol-3-yl)-(2-phenylquinazolin-4-yl)amine; 11) Purvalanol-A, or a combination thereof.

C. Agents that Affect Kinesin

In particular aspects of the invention, one or more agents that target kinesin is employed, and in specific aspects the one or more agents comprises an inhibitor of kinesin. The inhibitor may act directly on kinesin or may act indirectly on another molecule that affects kinesin. Any inhibitor of kinesin may be employed, although in specific embodiments the inhibitor comprises S-trityl-L-cysteine; 1,6,7,1′,6′,7′-Hexahydroxy-5,5′-diisopropyl-3,3′-dimethyl-[2,2′-binaphthalene]-8,8′-dicarboxaldehyde (also referred to as gossypol); 3-(5H-dibenzo[a,d]cyclohepten-5-ylidene)-N,N-dimethyl-1-1propanamine hydrochloride (also referred to as flexeril); 2-{[2-(4-{3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl}-1-piperazinyl)ethyl]amino}-ethanol trihydrochloride; K₆Mo₁₈O₆₂P₂; 2,3,4,5-Tetrabromo-6-(3,6-dihydroxy-9H-xanthen-9-yl)-benzoic acid; 1,1,2,2-Tetra(3,5-dichloro-4-hydroxyphenyl)ethane; 10-Carboxy-1,2,3,4,5,6,7,8,13,13,14,14-dodecachloro-1,4,4a,4b,5,8,8a,8b-octahydro-11,sulfo-1,4:5,8-demethanotriphenylene; 2,2′-Dithiobis-(8-quinolinol); 8-[3-(2-Chloro-10H-phenothiazin-10-yl)propyl]-8-azabicyclo[3.2.1]octane-3-ol, compound with ethanesulfonic acid, or a mixture or combination thereof, for example. (See DeBonis et al., 2004, for example, which is incorporated by reference herein in its entirety).

D. Agents that Affect Adenomatous Polyposis Coli Protein (APC)

In some embodiments of the invention, one or more agents that affect APC are employed in the invention. APC is one of the targets of GSK-3b phosphorylation and regulates microtubule capture at the actin cortex (a network of actin filaments beneath the plasma membrane). The mutated form of APC that is found in cancers most often loses its microtubule binding domain. In some embodiments, if APC fails to capture microtubules at the actin cortex, the microtubules extend past the plasma membrane to produce the observed protrusions associated with the invention. Thus, in specific embodiments any compound or therapy targeting the restoration of APC function will inhibit the protrusions. In particular embodiments, the compound comprises protein, peptide, nucleic acid, including DNA, RNA, small molecule, or a mixture or combination thereof, and so forth.

E. Inhibitors of Vimentin

In certain embodiments of the invention, one or more inhibitors of vimentin, such as vimentin assembly, are utilized, such as the following: 1) Calyculin-A; 2) Ionomycin; 3) ProstagladinF (2a); 4) Vimentin siRNA; 5) bradykinin; 6) Bisindolymaleimide; 7) Estramustine; 8) Isoproterenol; 9) 8-Br-cAMP; 10) epinephrine; 11) forskolin; 12) Prostaglandin-E1, or combinations thereof.

F. Inhibitors of Kinesin

In certain embodiments of the invention, one or more inhibitors of kinesin, such as kinesin activity, are employed, such as the following: 1) Lidocaine; 2) Tetracaine; 3) S-Trityl-L-cysteine; 4) Monastrol; 5) Adociasulfate-2; 6) Terpendole-E; 7) siRNAs against specific kinesins, or a combination thereof.

G. Inhibitors of Src

In certain embodiments of the invention, one or more inhibitors of Src, such as Src activity, are employed, such as follows: 1) 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine (PP2); 2) 4-(4′-Phenoxyanilino)-6,7-dimethoxyquinazoline; 3) Dasatinib; 4) Csk overexpression; 5) siRNA against Src, or a combination thereof.

H. Stabilizers of Actin

In certain embodiments of the invention, one or more stabilizers of actin, such as, for example, one or more of the following: 1) Jasplakinolide; 2) Phalloidin; 3) Dolastatin; 4) Chrondramides; 5) Doliculide, or a combination thereof.

IV. Antisense/siRNA Embodiments

TABLE I List of human kinesin/dynein names, Genbank accession numbers and PCR primer sequences for PCR amplification of DNA templates for generating siRNA_(s) SEQ ID SEQ ID Kinesin* Other name** GenBank ID Family** 5′ primer NO 3′ primer NO KIF 1A HsATSV NM_004321 Kinesin-3 GCGTAATACGACTCACTATAGGGGCAGGCCCAGCCCATCCCCT  77 GCGTAATACGACTCACTATAGGTTGGGAGACACATGTGGGAAC 119 KIF 1B HsKIF1B NM_015074 Kinesin-3 GCGTAATACGACTCACTATAGGCTCACTCGCCTTCGAGAGATA  78 GCGTAATACGACTCACTATAGGGATGTCTCCTCCCTTAGTCTC 120 KIF 1C HsKIF1C AB014606 Kinesin-3 GCGTAATACGACTCACTATAGGCTTGCTAGGAGAAGGGAAGAC  79 GCGTAATACGACTCACTATAGGAGGGGAGGGGAATGACTTATG 121 KIF 2A HsKin2 NM_004520 Kinesin-13 GCGTAATACGACTCACTATAGGAAGGATACCCAGAACCCTCAC  80 GCGTAATACGACTCACTATAGGGGAGTGGGCAAGGTATGTACA 122 KIF 2B HsLOC8464 NM_032559 Kinesin-13 GCGTAATACGACTCACTATAGGGAGATCAGGTCCGAAATGCTG  81 GCGTAATACGACTCACTATAGGAACCCCACCCACGGAACAACT 123 KIF 2C MCAK NM_006845 Kinesin-13 GCGTAATACGACTCACTATAGGCCAGAGAACTTTGGGTACCTG  82 GCGTAATACGACTCACTATAGGCTCTAGGGAGACAGTAAAGTA 124 KIF 3A HsKIF3A NM_007054 Kinesin-2 GCGTAATACGACTCACTATAGGGTGATATTCTCATGCCTGGAC  83 GCGTAATACGACTCACTATAGGCAGGCTGGGTGGGTGTTAGGA 125 KIF 3B HsKIF3B NM_004798 Kinesin-2 GCGTAATACGACTCACTATAGGGGGCGGAAACAGCATTTGCCT  84 GCGTAATACGACTCACTATAGGCTGATTCTGCCCTATTGTTCA 126 KIF 3C HsKIF3C NM_002254 Kinesin-2 GCGTAATACGACTCACTATAGGCAATAGACTCCTGGGATGGGG  85 GCGTAATACGACTCACTATAGGAGAAGATGGAGGTTATGGAGT 127 KIF 4A HsKIF4 AF071592 Kinesin-4 GCGTAATACGACTCACTATAGGCCCCAGTCTGGCTTGGGAGAT  86 GCGTAATACGACTCACTATAGGACATGGCAGACAATCAAGAGT 128 KIF 4B — AF241316 Kinesin-4 GCGTAATACGACTCACTATAGGGTTGGAGTCATCATCTCTACC  87 GCGTAATACGACTCACTATAGGAGGAACTTGATCATACTGAGG 129 KIF 5A HsnKHC NM_004984 Kinesin-1 GCGTAATACGACTCACTATAGGCTCTTACTTACTCTGTATCTC  88 GCGTAATACGACTCACTATAGGGCTATATGTGAAAGAGGAGGG 130 KIF 5B HsuKHC NM_004521 Kinesin-1 GCGTAATACGACTCACTATAGGGTAATCGAAGTACGAAGAGGA  89 GCGTAATACGACTCACTATAGGGCACAGTCCTATAAGGTAGAG 131 KIF 5C HsxKHC NM_004522 Kinesin-1 GCGTAATACGACTCACTATAGGGACTCCACGTAGCATGTCAAG  90 GCGTAATACGACTCACTATAGGGATCATCTGCCTCCACGGCAC 132 KIF 6 — BX649045 GCGTAATACGACTCACTATAGGGCCAGCAAGAACGAAGCACAG  91 GCGTAATACGACTCACTATAGGATGGTGCTATTTCACATTCTC 133 KIF 7 HsKIF7 NM_017576 TBD GCGTAATACGACTCACTATAGGAGATTCCTTTTTCTAACCTGT  92 GCGTAATACGACTCACTATAGGAGCAAGATTTAGCTGGATCTT 134 KIF 9 HsKIF9 NM_022342 Orphan GCGTAATACGACTCACTATAGGAGTACCTTAAAGGACAAGACC  93 GCGTAATACGACTCACTATAGGAGCCTGGCTGAGCTACTTTTC 135 KIF 10 HsCENP-E NM_001813 Kinesin-7 GCGTAATACGACTCACTATAGGCACTTCTCTGGAGATCCAGCA  94 GCGTAATACGACTCACTATAGGGAAGAGCGGTGATTCAGAACT 136 KIF 11 HsKPS/Eg5 NM_004523 Kinesin-5 GCGTAATACGACTCACTATAGGCTTGAACCCAGGAAGCGGGGT  95 GCGTAATACGACTCACTATAGGTCTAAGGACAGATGTTGGTGA 137 KIF 12 HsKIF12 NM_138424 TBD GCGTAATACGACTCACTATAGGGGCCAAGTGGGAACCCAGGAG  96 GCGTAATACGACTCACTATAGGAACCATGAAAGGAGATGGGAG 138 KIF13A HsRBKIN1 NM_022113 Kinesin-3 GCGTAATACGACTCACTATAGGGTCTAACTGTATGTCAACCCC  97 GCGTAATACGACTCACTATAGGTGACAGAGTTTAATTGGCAGT 139 KIF13B HsGAKIN AF279865 Kinesin-3 GCGTAATACGACTCACTATAGGCCCTGAGGAGCCAGGAGCCCG  98 GCGTAATACGACTCACTATAGGCAGAGGCACTTTGCGGGAAAC 140 KIF 14 HUMORFW D26361 Kinesin-3 GCGTAATACGACTCACTATAGGGGCACTTTTATGACCACCCAT  99 GCGTAATACGACTCACTATAGGGACTAAGTCTCGTTCTGTTGC 141 KIF 15 HsKip7 AB035898 Orphan GCGTAATACGACTCACTATAGGCCTAGGCATCACCTTGTTTGA 100 GCGTAATACGACTCACTATAGGGCTTCTTGTACCTGCTACTAA 142 KIF16A HsKIF16A AK122666 TBD GCGTAATACGACTCACTATAGGGTGGGATGCCAGAGCTGGATC 101 GCGTAATACGACTCACTATAGGTCTACTCCCTCATCATCTGGA 143 KIF16B HsJ777L9 AY166853 Kinesin-3 GCGTAATACGACTCACTATAGGGGAGGAACCACCACAGCAGTG 102 GCGTAATACGACTCACTATAGGGGAATATAGCCAGCCACATGG 144 KIF 17 HsKIAA1405 XM_027915 Kinesin-2 GCGTAATACGACTCACTATAGGGCCTTATAGGCATGTAGAGAC 103 GCGTAATACGACTCACTATAGGGTGCTTAGGAAGTGGGGCCAG 145 KIF18 HsDKFZp434 NM_031217 Kinesin-8 GCGTAATACGACTCACTATAGGCCAAGCAAAATGAAGTTGATC 104 GCGTAATACGACTCACTATAGGTCTTGGGCCATAATTTTACCA 146 KIF19A HsFLJ3730 AK094619 Orphan GCGTAATACGACTCACTATAGGGAGGCAAGGCGGAGGGGCCAG 105 GCGTAATACGACTCACTATAGGGTAAAGACGGGATTTCGCCAT 147 KIF20A HsRabK6/MKLP2 NM_005733 Kinesin-6 GCGTAATACGACTCACTATAGGGAGCAGTCATGGCCCTGAGGT 106 GCGTAATACGACTCACTATAGGTAGTTACTGGTCTCCACTGCC 148 KIF20B HsKlpMPP1 NM_016195 Orphan GCGTAATACGACTCACTATAGGGTCATAGTCATTGGAACTTGC 107 GCGTAATACGACTCACTATAGGCTGTACACACTTATTCTCCAA 149 KIF21A HsNYREN62 NM_017641 Kinesin-4 GCGTAATACGACTCACTATAGGGGTTGTAAACTGAATGCTGTG 108 GCGTAATACGACTCACTATAGGATGAATGAGTTAATGGTGGGC 150 KIF 22 HsKid NM_007317 Kinesin-10 GCGTAATACGACTCACTATAGGCCTCACTCCGCCTTTTCAAAT 109 GCGTAATACGACTCACTATAGGCAAGGCCGCCGTCGTTGCCGA 151 KIF 23 HsMKLP1 NM_004856 Kinesin-6 GCGTAATACGACTCACTATAGGGTCCCAGTACTGAAAGAACAT 110 GCGTAATACGACTCACTATAGGGACCAGGGCTGGAGAAGTCAC 152 KIF 24 — NM_018278 GCGTAATACGACTCACTATAGGGAGGGAAAGTAGCCTCAGGCA 111 GCGTAATACGACTCACTATAGGTGTAGGTGAACTAACTGCCCC 153 KIF 25 HsKlp6q27 NM_005355 unamed GCGTAATACGACTCACTATAGGCAGCAAGTAAGCAGAAGACTC 112 GCGTAATACGACTCACTATAGGGCATGAGCCACCATGCCTGGC 154 KIF26A HsKIAA1236 XM_050278 Orphan GCGTAATACGACTCACTATAGGGACAAGAGGAGGGGGCGTGCA 113 GCGTAATACGACTCACTATAGGTAAGTCCCACTCCACTCCACA 155 KIF26B HsLOC3489 BC035896 Orphan GCGTAATACGACTCACTATAGGGGGTACCTACCCTCATGACCT 114 GCGTAATACGACTCACTATAGGTTAGCCAGGCACGGTGGTGCA 156 KIF C1 HsCHO2 XM_058039 Kinesin-14 GCGTAATACGACTCACTATAGGCGGATCCAGATCTGTGTGTGT 115 GCGTAATACGACTCACTATAGGGTGGATAGCTAGAGGGCACAC 157 KIF C2 HsKIFC2 NM_145754 Kinesin-14 GCGTAATACGACTCACTATAGGGTCTCCCAGGGCACAAGCTCC 116 GCGTAATACGACTCACTATAGGGTCTGGAAAGGAGGTAGCACC 158 KIF C3 HsKIFC3 NM_005550 Kinesin-14 GCGTAATACGACTCACTATAGGGCCTGAAGCTGGGCCCTCACT 117 GCGTAATACGACTCACTATAGGATGGGTCTTGGGTCTGCCCAG 159 DYNEIN DHC1 BC021297 GCGTAATACGACTCACTATAGGGCCCCTTTCTGTAATAGTGAA 118 GCGTAATACGACTCACTATAGGGTGTCTGTGAAGGGCCCCAAG 160 *see reference Miki et al. **see reference Lawrence et al.

Molecules directed against a transcript may be employed to inhibit the expression of the product, for example. The molecules may be of any suitable length, and in specific embodiments the molecules are antisense RNA molecules, for example that may be as long as the full length of an mRNA or shorter. In specific embodiments, siRNA is employed, which usually refers to shorter versions 21-23 bp in length. This shorter version usually helps the cell avoid mounting an antiviral response (interferon-based) to the dsRNA molecule. Since dsRNAs look a lot like some retroviruses, cells have an intricate system to shut the cell down (and even commit apoptosis) if a dsRNA that is too long appears in the cytoplasm. The shorter 21-23 bp fragment essentially elude this system, since the cell has probably decided that something this short cannot be a viral threat.

Antisense, including siRNA, molecules may be generated against any suitable polynucleotide to inhibit microtubule protrusions. In specific embodiments, exemplary sequences provided herein. In specific embodiments, the antisense, including siRNA, molecules may be directed against a 5′ leader, exon, intron, splice junction, or 3′ UTR, for example. They may be of any suitable length, although in specific embodiments they are 21, 22, or 23 base pairs in length.

For example, one may employ vimentin polynucleotides to obtain exemplary antisense or siRNA molecules: NM_(—)003380 (SEQ ID NO:1), BC066956 (SEQ ID NO:2), BC030573 (SEQ ID NO:3), or BC000163 (SEQ ID NO:4). An exemplary GSK-3b polynucleotide to obtain exemplary antisense or siRNA molecules includes NM_(—)002093 (SEQ ID NO:5). An exemplary c-Src polynucleotide to obtain exemplary antisense or siRNA molecules includes BC104847 (SEQ ID NO:6). Exemplary Fyn polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)153048 (SEQ ID NO:7), NM_(—)153047 (SEQ ID NO:8), or NM_(—)002037 (SEQ ID NO:9). An exemplary Fer polynucleotide to obtain exemplary antisense or siRNA molecules includes NM_(—)005246 (SEQ ID NO:10). Exemplary Lck polynucleotides to obtain exemplary antisense or siRNA molecules includes NM_(—)001042771 (SEQ ID NO:11) or NM_(—)005356 (SEQ ID NO:12). An exemplary c-Yes polynucleotide to obtain exemplary antisense or siRNA molecules includes NM_(—)005433 (SEQ ID NO:13). Exemplary Fgr polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)005248 (SEQ ID NO:14), NM_(—)001042747 (SEQ ID NO:15), or NM_(—)001042729 (SEQ ID NO:16). An exemplary Lyn polynucleotide to obtain exemplary antisense or siRNA molecules includes NM_(—)002350 (SEQ ID NO:17). Exemplary Hck polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)002110 (SEQ ID NO:18) and AY893634 (SEQ ID NO:19). Exemplary Blk polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)001715 (SEQ ID NO:20), BC032413 (SEQ ID NO:21), or BC007371 (SEQ ID NO:22). Exemplary c-Abl polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)005157 (SEQ ID NO:23), NM_(—)007313 (SEQ ID NO:24), NM_(—)005158 (SEQ ID NO:25), or M14752 (SEQ ID NO:26). Exemplary hAGTPBP1 polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)015239 (SEQ ID NO:27) or BC060815 (SEQ ID NO:28). Exemplary hAGBL2 polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)024783 (SEQ ID NO:29), BC036234 (SEQ ID NO:30), or BC028200 (SEQ ID NO:31). An exemplary hAGBL3 polynucleotide to obtain exemplary antisense or siRNA molecules includes BC030651 (SEQ ID NO:32). Exemplary hAGBL4 polynucleotides to obtain exemplary antisense or siRNA molecules include NM_(—)032785 (SEQ ID NO:33) or BC126383 (SEQ ID NO:34).

Exemplary kinesin polynucleotides sequences are provided, such as those that are suitable for targeting antisense or siRNA molecules against: KIF 1A (NM_(—)004321; SEQ ID NO:35); KIF 1B (NM_(—)015074; SEQ ID NO:36); KIF 1C (AB014606; SEQ ID NO:37); KIF 2A (NM_(—)004520; SEQ ID NO:38); KIF 2B (NM_(—)032559; SEQ ID NO:39); KIF 2C (NM_(—)006845; SEQ ID NO:40); KIF 3A (NM_(—)007054; SEQ ID NO:41); KIF 3B (NM_(—)004798; SEQ ID NO:42); KIF 3C(NM_(—)002254; SEQ ID NO:43); KIF 4A (AF071592; SEQ ID NO:44); KIF 4B (AF241316; SEQ ID NO:45); KIF 5A (NM_(—)004984; SEQ ID NO:46); KIF 5B (NM_(—)004521; SEQ ID NO:47); KIF 5C(NM_(—)004522; SEQ ID NO:48); KIF 6 (BX649045; SEQ ID NO:49); KIF 7 (NM_(—)017576; SEQ ID NO:50); KIF 9 (NM_(—)022342; SEQ ID NO:51); KIF 10 (NM_(—)001813; SEQ ID NO:52); KIF 11 (NM_(—)004523; SEQ ID NO:53); KIF 12 (NM_(—)138424; SEQ ID NO:54); KIF13A (NM_(—)022113; SEQ ID NO:55); KIF13B (AF279865; SEQ ID NO:56); KIF 14 (D26361; SEQ ID NO:57); KIF 15 (AB035898; SEQ ID NO:58); KIF16A (AK122666; SEQ ID NO:59); KIF16B (AY166853; SEQ ID NO:60); KIF 17 (XM_(—)027915; SEQ ID NO:61); KIF18 (NM_(—)031217; SEQ ID NO:62); KIF19A (AK094619; SEQ ID NO:63); KIF20A (NM_(—)005733; SEQ ID NO:64); KIF20B (NM_(—)016195; SEQ ID NO:65); KIF21A (NM_(—)017641; SEQ ID NO:66); KIF 22 (NM_(—)007317; SEQ ID NO:67); KIF 23 (NM_(—)004856; SEQ ID NO:68); KIF 24 (NM_(—)018278; SEQ ID NO:69); KIF 25 (NM_(—)005355; SEQ ID NO:70); KIF26A (XM_(—)050278; SEQ ID NO:71); KIF26B (BC035896; SEQ ID NO:72); KIF C1 (XM_(—)058039; SEQ ID NO:73); KIF C2 (NM_(—)145754; SEQ ID NO:74); KIF C3 (NM_(—)005550; SEQ ID NO:75); and DYNEIN (BC021297; SEQ ID NO:76).

V. Combination Therapy

In certain embodiments of the invention, an individual receiving cancer therapy of the present invention or an individual that will receive cancer therapy of the present invention also receives an additional cancer therapy. In some instances, the additional therapy targets the primary cancer in the individual, whereas in other instances the additional therapy targets cancer that has metastasized, or both. The inventive therapy may be used during the treatment of the primary tumor and thus be employed at the same time as an additional treatment for the cancer.

Thus, in certain embodiments of the invention, it is desirable to combine the inventive compositions with other agents effective in the treatment of hyperproliferative disease, such as anti-cancer agents. In particular embodiments, an anti-cancer agent includes a composition of the invention. An “anti-cancer” agent is capable of negatively affecting cancer in a subject, for example, by killing cancer cells, inducing apoptosis in cancer cells, reducing the growth rate of cancer cells, reducing the incidence or number of metastases, reducing tumor size, inhibiting tumor growth, reducing the blood supply to a tumor or cancer cells, promoting an immune response against cancer cells or a tumor, preventing or inhibiting the progression of cancer, or increasing the lifespan of a subject with cancer.

More generally, these other compositions would be provided in a combined amount effective to kill or inhibit proliferation of the cell. This process may involve contacting the cells with the inventive agent and the additional agent(s) or multiple factor(s) at the same time. This may be achieved by contacting the cell with a single composition or pharmacological formulation that includes both agents, or by contacting the cell with two distinct compositions or formulations, at the same time, wherein one composition includes the agent of the invention and the other includes the second agent(s).

Tumor cell resistance to chemotherapy and radiotherapy agents represents a major problem in clinical oncology. One goal of current cancer research is to find ways to improve the efficacy of chemo- and radiotherapy by combining it with another therapy. For example, the herpes simplex-thymidine kinase (HS-tK) gene, when delivered to brain tumors by a retroviral vector system, successfully induced susceptibility to the antiviral agent ganciclovir (Culver, et al., 1992). In the context of the present invention, it is contemplated that the inventive therapy could be used similarly in conjunction with chemotherapeutic, radiotherapeutic, or immunotherapeutic intervention, in addition to pro-apoptotic or cell cycle regulating agents, for example.

In one specific embodiment, localized heating may be employed as a therapy in addition to the inventive therapy, and in specific embodiments the localized heating facilitates directly or indirectly the release of a tumor cell from a primary tumor mass. One current tumor treatment is to use an approach such as focal ultrasound or heating of nanoparticles with magnetic fields to heat the local environment surrounding a tumor or the tumor cells themselves. Like focused radiation or laser-based photodynamic therapy, such a heat-based treatment could destroy most of a given tumor, but also promote the spread of the cells that survive the treatment (as can any cancer therapy, in particular aspects of the invention). The subsequent healing process (growth factors, motility stimulation and angiogenesis, for example) could also promote the spread of the tumor cells away from the primary site, similar to surgery. Thus, tissue-damaging types of treatments may be employed with the inventive therapy of inhibition of microtubule protrusions.

The inventive therapy may precede or follow the other agent treatment by intervals ranging from minutes to weeks. In embodiments where the other agent and agent of the invention are applied separately to the cell, one would generally ensure that a significant period of time did not expire between the time of each delivery, such that the agent and additional therapy would still be able to exert an advantageously combined effect on the cell. In such instances, it is contemplated that one may contact the cell with both modalities within about 12-24 h of each other and, more preferably, within about 6-12 h of each other. In some situations, it may be desirable to extend the time period for treatment significantly, however, where several d (2, 3, 4, 5, 6 or 7) to several wk (1, 2, 3, 4, 5, 6, 7 or 8) lapse between the respective administrations.

Various combinations may be employed, wherein agent of the invention is “A” and the secondary agent, such as radio- or chemotherapy, for example, is “B”:

A/B/A B/A/B B/B/A A/A/B A/B/B B/A/A A/B/B/B B/A/B/B B/B/B/A B/B/A/B A/A/B/B A/B/A/B A/B/B/A B/B/A/A B/A/B/A B/A/A/B A/A/A/B B/A/A/A A/B/A/A A/A/B/A

Administration of the therapeutic agents of the present invention to an individual will follow general protocols for the administration of chemotherapeutics, taking into account the toxicity, if any, of the agent. It is expected that the treatment cycles would be repeated as necessary. It also is contemplated that various standard therapies, as well as surgical intervention, may be applied in combination with the described hyperproliferative cell therapy.

A. Chemotherapy

Cancer therapies also include a variety of combination therapies with both chemical- and radiation-based treatments. Combination chemotherapies include, for example, cisplatin (CDDP), carboplatin, procarbazine, mechlorethamine, cyclophosphamide, camptothecin, ifosfamide, melphalan, chlorambucil, busulfan, nitrosurea, dactinomycin, daunorubicin, doxorubicin, bleomycin, plicomycin, mitomycin, etoposide (VP16), tamoxifen, raloxifene, estrogen receptor binding agents, taxol, gemcitabien, navelbine, farnesyl-protein transferase inhibitors, transplatinum, 5-fluorouracil, vincristin, vinblastin and methotrexate, or any analog or derivative variant of the foregoing.

B. Radiotherapy

Other factors that cause DNA damage and have been used extensively include what are commonly known as γ-rays, X-rays, and/or the directed delivery of radioisotopes to tumor cells. Other forms of DNA damaging factors are also contemplated such as microwaves and UV-irradiation. It is most likely that all of these factors effect a broad range of damage on DNA, on the precursors of DNA, on the replication and repair of DNA, and on the assembly and maintenance of chromosomes. Dosage ranges for X-rays range from daily doses of 50 to 200 roentgens for prolonged periods of time (3 to 4 wk), to single doses of 2000 to 6000 roentgens. Dosage ranges for radioisotopes vary widely, and depend on the half-life of the isotope, the strength and type of radiation emitted, and the uptake by the neoplastic cells.

The terms “contacted” and “exposed,” when applied to a cell, are used herein to describe the process by which a therapeutic construct and a chemotherapeutic or radiotherapeutic agent are delivered to a target cell or are placed in direct juxtaposition with the target cell. To achieve cell killing or stasis, both agents are delivered to a cell in a combined amount effective to kill the cell or prevent it from dividing.

C. Immunotherapy

Immunotherapeutics, generally, rely on the use of immune effector cells and molecules to target and destroy cancer cells. The immune effector may be, for example, an antibody specific for some marker on the surface of a tumor cell. The antibody alone may serve as an effector of therapy or it may recruit other cells to actually effect cell killing. The antibody also may be conjugated to a drug or toxin (chemotherapeutic, radionuclide, ricin A chain, cholera toxin, pertussis toxin, etc.) and serve merely as a targeting agent. Alternatively, the effector may be a lymphocyte carrying a surface molecule that interacts, either directly or indirectly, with a tumor cell target. Various effector cells include cytotoxic T cells and NK cells.

Immunotherapy, thus, could be used as part of a combined therapy, in conjunction with an agent of the invention. The general approach for combined therapy is discussed below. Generally, the tumor cell must bear some marker that is amenable to targeting, i.e., is not present on the majority of other cells. Many tumor markers exist and any of these may be suitable for targeting in the context of the present invention. Common tumor markers include carcinoembryonic antigen, prostate specific antigen, urinary tumor associated antigen, fetal antigen, tyrosinase (p97), gp68, TAG-72, HMFG, Sialyl Lewis Antigen, MucA, MucB, PLAP, estrogen receptor, laminin receptor, erb B and p155.

D. Genes

In yet another embodiment, the additional treatment is a gene therapy in which a therapeutic polynucleotide is administered before, after, or at the same time as an agent of the invention. A variety of proteins are encompassed within the invention, some of which are described below.

1. Inducers of Cellular Proliferation

The proteins that induce cellular proliferation further fall into various categories dependent on function. The commonality of all of these proteins is their ability to regulate cellular proliferation. For example, a form of PDGF, the sis oncogene, is a secreted growth factor. Oncogenes rarely arise from genes encoding growth factors, and at the present, sis is the only known naturally-occurring oncogenic growth factor. In one embodiment of the present invention, it is contemplated that anti-sense mRNA directed to a particular inducer of cellular proliferation is used to prevent expression of the inducer of cellular proliferation.

The proteins FMS, ErbA, ErbB and neu are growth factor receptors. Mutations to these receptors result in loss of regulatable function. For example, a point mutation affecting the transmembrane domain of the Neu receptor protein results in the neu oncogene. The erbA oncogene is derived from the intracellular receptor for thyroid hormone. The modified oncogenic ErbA receptor is believed to compete with the endogenous thyroid hormone receptor, causing uncontrolled growth.

The largest class of oncogenes includes the signal transducing proteins (e.g., Src, Abl and Ras). The protein Src is a cytoplasmic protein-tyrosine kinase, and its transformation from proto-oncogene to oncogene in some cases, results via mutations at tyrosine residue 527. In contrast, transformation of GTPase protein ras from proto-oncogene to oncogene, in one example, results from a valine to glycine mutation at amino acid 12 in the sequence, reducing ras GTPase activity.

The proteins Jun, Fos and Myc are proteins that directly exert their effects on nuclear functions as transcription factors.

2. Inhibitors of Cellular Proliferation

The tumor suppressor oncogenes function to inhibit excessive cellular proliferation. The inactivation of these genes destroys their inhibitory activity, resulting in unregulated proliferation. The tumor suppressors p53, p16 and C-CAM are described below.

High levels of mutant p53 have been found in many cells transformed by chemical carcinogenesis, ultraviolet radiation, and several viruses. The p53 gene is a frequent target of mutational inactivation in a wide variety of human tumors and is already documented to be the most frequently mutated gene in common human cancers. It is mutated in over 50% of human NSCLC (Hollstein et al., 1991) and in a wide spectrum of other tumors.

The p53 gene encodes a 393-amino acid phosphoprotein that can form complexes with host proteins such as large-T antigen and E1B. The protein is found in normal tissues and cells, but at concentrations which are minute by comparison with transformed cells or tumor tissue

Wild-type p53 is recognized as an important growth regulator in many cell types. Missense mutations are common for the p53 gene and are essential for the transforming ability of the oncogene. A single genetic change prompted by point mutations can create carcinogenic p53. Unlike other oncogenes, however, p53 point mutations are known to occur in at least 30 distinct codons, often creating dominant alleles that produce shifts in cell phenotype without a reduction to homozygosity. Additionally, many of these dominant negative alleles appear to be tolerated in the organism and passed on in the germ line. Various mutant alleles appear to range from minimally dysfunctional to strongly penetrant, dominant negative alleles (Weinberg, 1991).

Another inhibitor of cellular proliferation is p16. The major transitions of the eukaryotic cell cycle are triggered by cyclin-dependent kinases, or CDK'S. One CDK, cyclin-dependent kinase 4 (CDK4), regulates progression through the G1. The activity of this enzyme may be to phosphorylate Rb at late G1. The activity of CDK4 is controlled by an activating subunit, D-type cyclin, and by an inhibitory subunit, the p16INK4 has been biochemically characterized as a protein that specifically binds to and inhibits CDK4, and thus may regulate Rb phosphorylation (Serrano et al., 1993; Serrano et al., 1995). Since the p16INK4 protein is a CDK4 inhibitor (Serrano, 1993), deletion of this gene may increase the activity of CDK4, resulting in hyperphosphorylation of the Rb protein. p16 also is known to regulate the function of CDK6.

p16INK4 belongs to a newly described class of CDK-inhibitory proteins that also includes p16B, p19, p21WAF1, and p27KIP1. The p16INK4 gene maps to 9p21, a chromosome region frequently deleted in many tumor types. Homozygous deletions and mutations of the p16INK4 gene are frequent in human tumor cell lines. This evidence suggests that the p16INK4 gene is a tumor suppressor gene. This interpretation has been challenged, however, by the observation that the frequency of the p16INK4 gene alterations is much lower in primary uncultured tumors than in cultured cell lines (Caldas et al., 1994; Cheng et al., 1994; Hussussian et al., 1994; Kamb et al., 1994; Kamb et al., 1994; Mori et al., 1994; Okamoto et al., 1994; Nobori et al., 1995; Orlow et al., 1994; Arap et al., 1995). Restoration of wild-type p16INK4 function by transfection with a plasmid expression vector reduced colony formation by some human cancer cell lines (Okamoto, 1994; Arap, 1995).

Other genes that may be employed according to the present invention include Rb, APC, DCC, NF-1, NF-2, WT-1, MEN-I, MEN-II, zac1, p73, VHL, MMAC1/PTEN, DBCCR-1, FCC, rsk-3, p27, p27/p16 fusions, p21/p27 fusions, anti-thrombotic genes (e.g., COX-1, TFPI), PGS, Dp, E2F, ras, myc, neu, raf, erb, fms, trk, ret, gsp, hst, abl, E1A, p300, genes involved in angiogenesis (e.g., VEGF, FGF, thrombospondin, BAI-1, GDAIF, or their receptors) and MCC.

3. Regulators of Programmed Cell Death

Apoptosis, or programmed cell death, is an essential process for normal embryonic development, maintaining homeostasis in adult tissues, and suppressing carcinogenesis (Kerr et al., 1972). The Bcl-2 family of proteins and ICE-like proteases have been demonstrated to be important regulators and effectors of apoptosis in other systems. The Bcl-2 protein, discovered in association with follicular lymphoma, plays a prominent role in controlling apoptosis and enhancing cell survival in response to diverse apoptotic stimuli (Bakhshi et al., 1985; Cleary and Sklar, 1985; Cleary et al., 1986; Tsujimoto et al., 1985; Tsujimoto and Croce, 1986). The evolutionarily conserved Bcl-2 protein now is recognized to be a member of a family of related proteins, which can be categorized as death agonists or death antagonists.

Subsequent to its discovery, it was shown that Bcl-2 acts to suppress cell death triggered by a variety of stimuli. Also, it now is apparent that there is a family of Bcl-2 cell death regulatory proteins which share in common structural and sequence homologies. These different family members have been shown to either possess similar functions to Bcl-2 (e.g., BclXL, BclW, BclS, Mcl-1, A1, Bfl-1) or counteract Bcl-2 function and promote cell death (e.g., Bax, Bak, Bik, Bim, Bid, Bad, Harakiri).

E. Surgery

Approximately 60% of persons with cancer will undergo surgery of some type, which includes preventative, diagnostic or staging, curative and palliative surgery. Curative surgery is a cancer treatment that may be used in conjunction with other therapies, such as the treatment of the present invention, chemotherapy, radiotherapy, hormonal therapy, gene therapy, immunotherapy and/or alternative therapies.

Curative surgery includes resection in which all or part of cancerous tissue is physically removed, excised, and/or destroyed. Tumor resection refers to physical removal of at least part of a tumor. In addition to tumor resection, treatment by surgery includes laser surgery, cryosurgery, electrosurgery, and microscopically controlled surgery (Mohs' surgery). It is further contemplated that the present invention may be used in conjunction with removal of superficial cancers, precancers, or incidental amounts of normal tissue.

Upon excision of part of all of cancerous cells, tissue, or tumor, a cavity may be formed in the body. Treatment may be accomplished by perfusion, direct injection or local application of the area with an additional anti-cancer therapy. Such treatment may be repeated, for example, every 1, 2, 3, 4, 5, 6, or 7 days, or every 1, 2, 3, 4, and 5 weeks or every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months. These treatments may be of varying dosages as well.

F. Other Agents

It is contemplated that other agents may be used in combination with the present invention to improve the therapeutic efficacy of treatment. These additional agents include immunomodulatory agents, agents that affect the upregulation of cell surface receptors and GAP junctions, cytostatic and differentiation agents, inhibitors of cell adhesion, or agents that increase the sensitivity of the hyperproliferative cells to apoptotic inducers. Immunomodulatory agents include tumor necrosis factor; interferon alpha, beta, and gamma; IL-2 and other cytokines; F42K and other cytokine analogs; or MIP-1, MIP-1beta, MCP-1, RANTES, and other chemokines. It is further contemplated that the upregulation of cell surface receptors or their ligands such as Fas/Fas ligand, DR4 or DR5/TRAIL would potentiate the apoptotic inducing abilities of the present invention by establishment of an autocrine or paracrine effect on hyperproliferative cells. Increases intercellular signaling by elevating the number of GAP junctions would increase the anti-hyperproliferative effects on the neighboring hyperproliferative cell population. In other embodiments, cytostatic or differentiation agents can be used in combination with the present invention to improve the anti-hyerproliferative efficacy of the treatments. Inhibitors of cell adhesion are contemplated to improve the efficacy of the present invention. Examples of cell adhesion inhibitors are focal adhesion kinase (FAKs) inhibitors and Lovastatin. It is further contemplated that other agents that increase the sensitivity of a hyperproliferative cell to apoptosis, such as the antibody c225, could be used in combination with the present invention to improve the treatment efficacy.

Hormonal therapy may also be used in conjunction with the present invention or in combination with any other cancer therapy previously described. The use of hormones may be employed in the treatment of certain cancers such as breast, prostate, ovarian, or cervical cancer to lower the level or block the effects of certain hormones such as testosterone or estrogen. This treatment is often used in combination with at least one other cancer therapy as a treatment option or to reduce the risk of metastases.

VI. Pharmaceutical Preparations

Pharmaceutical compositions of the present invention comprise an effective amount of one or more agents of the invention and, optionally, additional agents, dissolved or dispersed in or provided with a pharmaceutically acceptable carrier, for example. The phrases “pharmaceutical or pharmacologically acceptable” refers to molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to an animal, such as, for example, a human, as appropriate. The preparation of an pharmaceutical composition that contains at least one agent of the invention or additional active ingredient will be known to those of skill in the art in light of the present disclosure, as exemplified by Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990, incorporated herein by reference. Moreover, for animal (e.g., human) administration, it will be understood that preparations should meet sterility, pyrogenicity, general safety and purity standards as required by FDA Office of Biological Standards.

As used herein, “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial agents, antifungal agents), isotonic agents, absorption delaying agents, salts, preservatives, drugs, drug stabilizers, gels, binders, excipients, disintegration agents, lubricants, sweetening agents, flavoring agents, dyes, such like materials and combinations thereof, as would be known to one of ordinary skill in the art (see, for example, Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990, pp. 1289-1329, incorporated herein by reference). Except insofar as any conventional carrier is incompatible with the active ingredient, its use in the pharmaceutical compositions is contemplated.

The agent of the invention may comprise different types of carriers depending on whether it is to be administered in solid, liquid or aerosol form, and whether it need to be sterile for such routes of administration as injection. The present invention can be administered intravenously, intradermally, transdermally, intrathecally, intraarterially, intraperitoneally, intranasally, intravaginally, intrarectally, topically, intramuscularly, subcutaneously, mucosally, orally, topically, locally, inhalation (e.g., aerosol inhalation), injection, infusion, continuous infusion, localized perfusion bathing target cells directly, via a catheter, via a lavage, in cremes, in lipid compositions (e.g., liposomes), or by other method or any combination of the forgoing as would be known to one of ordinary skill in the art (see, for example, Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990, incorporated herein by reference).

The agent of the invention may be formulated into a composition in a free base, neutral or salt form. Pharmaceutically acceptable salts, include the acid addition salts, e.g., those formed with the free amino groups of a proteinaceous composition, or which are formed with inorganic acids such as for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric or mandelic acid. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as for example, sodium, potassium, ammonium, calcium or ferric hydroxides; or such organic bases as isopropylamine, trimethylamine, histidine or procaine. Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective. The formulations are easily administered in a variety of dosage forms such as formulated for parenteral administrations such as injectable solutions, or aerosols for delivery to the lungs, or formulated for alimentary administrations such as drug release capsules and the like.

Further in accordance with the present invention, the composition of the present invention suitable for administration is provided in a pharmaceutically acceptable carrier with or without an inert diluent. The carrier should be assimilable and includes liquid, semi-solid, i.e., pastes, or solid carriers. Except insofar as any conventional media, agent, diluent or carrier is detrimental to the recipient or to the therapeutic effectiveness of a composition contained therein, its use in administrable composition for use in practicing the methods of the present invention is appropriate. Examples of carriers or diluents include fats, oils, water, saline solutions, lipids, liposomes, resins, binders, fillers and the like, or combinations thereof. The composition may also comprise various antioxidants to retard oxidation of one or more component. Additionally, the prevention of the action of microorganisms can be brought about by preservatives such as various antibacterial and antifungal agents, including but not limited to parabens (e.g., methylparabens, propylparabens), chlorobutanol, phenol, sorbic acid, thimerosal or combinations thereof.

In accordance with the present invention, the composition is combined with the carrier in any convenient and practical manner, i.e., by solution, suspension, emulsification, admixture, encapsulation, absorption and the like. Such procedures are routine for those skilled in the art.

In a specific embodiment of the present invention, the composition is combined or mixed thoroughly with a semi-solid or solid carrier. The mixing can be carried out in any convenient manner such as grinding. Stabilizing agents can be also added in the mixing process in order to protect the composition from loss of therapeutic activity, i.e., denaturation in the stomach. Examples of stabilizers for use in an the composition include buffers, amino acids such as glycine and lysine, carbohydrates such as dextrose, mannose, galactose, fructose, lactose, sucrose, maltose, sorbitol, mannitol, etc.

In further embodiments, the present invention may concern the use of a pharmaceutical lipid vehicle compositions that include the agent of the invention, one or more lipids, and an aqueous solvent. As used herein, the term “lipid” will be defined to include any of a broad range of substances that is characteristically insoluble in water and extractable with an organic solvent. This broad class of compounds is well known to those of skill in the art, and as the term “lipid” is used herein, it is not limited to any particular structure. Examples include compounds which contain long-chain aliphatic hydrocarbons and their derivatives. A lipid may be naturally occurring or synthetic (i.e., designed or produced by man). However, a lipid is usually a biological substance. Biological lipids are well known in the art, and include for example, neutral fats, phospholipids, phosphoglycerides, steroids, terpenes, lysolipids, glycosphingolipids, glycolipids, sulphatides, lipids with ether and ester-linked fatty acids and polymerizable lipids, and combinations thereof. Of course, compounds other than those specifically described herein that are understood by one of skill in the art as lipids are also encompassed by the compositions and methods of the present invention.

One of ordinary skill in the art would be familiar with the range of techniques that can be employed for dispersing a composition in a lipid vehicle. For example, the agent of the invention may be dispersed in a solution containing a lipid, dissolved with a lipid, emulsified with a lipid, mixed with a lipid, combined with a lipid, covalently bonded to a lipid, contained as a suspension in a lipid, contained or complexed with a micelle or liposome, or otherwise associated with a lipid or lipid structure by any means known to those of ordinary skill in the art. The dispersion may or may not result in the formation of liposomes.

The actual dosage amount of a composition of the present invention administered to an animal patient can be determined by physical and physiological factors such as body weight, severity of condition, the type of disease being treated, previous or concurrent therapeutic interventions, idiopathy of the patient and on the route of administration. Depending upon the dosage and the route of administration, the number of administrations of a preferred dosage and/or an effective amount may vary according to the response of the subject. The practitioner responsible for administration will, in any event, determine the concentration of active ingredient(s) in a composition and appropriate dose(s) for the individual subject.

In certain embodiments, pharmaceutical compositions may comprise, for example, at least about 0.1% of an active compound. In other embodiments, the an active compound may comprise between about 2% to about 75% of the weight of the unit, or between about 25% to about 60%, for example, and any range derivable therein. Naturally, the amount of active compound(s) in each therapeutically useful composition may be prepared is such a way that a suitable dosage will be obtained in any given unit dose of the compound. Factors such as solubility, bioavailability, biological half-life, route of administration, product shelf life, as well as other pharmacological considerations will be contemplated by one skilled in the art of preparing such pharmaceutical formulations, and as such, a variety of dosages and treatment regimens may be desirable.

In other non-limiting examples, a dose may also comprise from about 1 microgram/kg/body weight, about 5 microgram/kg/body weight, about 10 microgram/kg/body weight, about 50 microgram/kg/body weight, about 100 microgram/kg/body weight, about 200 microgram/kg/body weight, about 350 microgram/kg/body weight, about 500 microgram/kg/body weight, about 1 milligram/kg/body weight, about 5 milligram/kg/body weight, about 10 milligram/kg/body weight, about 50 milligram/kg/body weight, about 100 milligram/kg/body weight, about 200 milligram/kg/body weight, about 350 milligram/kg/body weight, about 500 milligram/kg/body weight, to about 1000 mg/kg/body weight or more per administration, and any range derivable therein. In non-limiting examples of a derivable range from the numbers listed herein, a range of about 5 mg/kg/body weight to about 100 mg/kg/body weight, about 5 microgram/kg/body weight to about 500 milligram/kg/body weight, etc., can be administered, based on the numbers described above.

A. Alimentary Compositions and Formulations

In preferred embodiments of the present invention, one or more agents of the invention are formulated to be administered via an alimentary route. Alimentary routes include all possible routes of administration in which the composition is in direct contact with the alimentary tract. Specifically, the pharmaceutical compositions disclosed herein may be administered orally, buccally, rectally, or sublingually. As such, these compositions may be formulated with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard- or soft-shell gelatin capsule, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet.

In certain embodiments, the active compounds may be incorporated with excipients and used in the form of ingestible tablets, buccal tables, troches, capsules, elixirs, suspensions, syrups, wafers, and the like (Mathiowitz et al., 1997; Hwang et al., 1998; U.S. Pat. Nos. 5,641,515; 5,580,579 and 5,792,451, each specifically incorporated herein by reference in its entirety). The tablets, troches, pills, capsules and the like may also contain the following: a binder, such as, for example, gum tragacanth, acacia, cornstarch, gelatin or combinations thereof; an excipient, such as, for example, dicalcium phosphate, mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate or combinations thereof; a disintegrating agent, such as, for example, corn starch, potato starch, alginic acid or combinations thereof; a lubricant, such as, for example, magnesium stearate; a sweetening agent, such as, for example, sucrose, lactose, saccharin or combinations thereof; a flavoring agent, such as, for example peppermint, oil of wintergreen, cherry flavoring, orange flavoring, etc. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar, or both. When the dosage form is a capsule, it may contain, in addition to materials of the above type, carriers such as a liquid carrier. Gelatin capsules, tablets, or pills may be enterically coated. Enteric coatings prevent denaturation of the composition in the stomach or upper bowel where the pH is acidic. See, e.g., U.S. Pat. No. 5,629,001. Upon reaching the small intestines, the basic pH therein dissolves the coating and permits the composition to be released and absorbed by specialized cells, e.g., epithelial enterocytes and Peyer's patch M cells. A syrup of elixir may contain the active compound sucrose as a sweetening agent methyl and propylparabens as preservatives, a dye and flavoring, such as cherry or orange flavor. Of course, any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, the active compounds may be incorporated into sustained-release preparation and formulations.

For oral administration the compositions of the present invention may alternatively be incorporated with one or more excipients in the form of a mouthwash, dentifrice, buccal tablet, oral spray, or sublingual orally-administered formulation. For example, a mouthwash may be prepared incorporating the active ingredient in the required amount in an appropriate solvent, such as a sodium borate solution (Dobell's Solution). Alternatively, the active ingredient may be incorporated into an oral solution such as one containing sodium borate, glycerin and potassium bicarbonate, or dispersed in a dentifrice, or added in a therapeutically-effective amount to a composition that may include water, binders, abrasives, flavoring agents, foaming agents, and humectants. Alternatively the compositions may be fashioned into a tablet or solution form that may be placed under the tongue or otherwise dissolved in the mouth.

Additional formulations which are suitable for other modes of alimentary administration include suppositories. Suppositories are solid dosage forms of various weights and shapes, usually medicated, for insertion into the rectum. After insertion, suppositories soften, melt or dissolve in the cavity fluids. In general, for suppositories, traditional carriers may include, for example, polyalkylene glycols, triglycerides or combinations thereof. In certain embodiments, suppositories may be formed from mixtures containing, for example, the active ingredient in the range of about 0.5% to about 10%, and preferably about 1% to about 2%.

B. Parenteral Compositions and Formulations

In further embodiments, an agent of the invention may be administered via a parenteral route. As used herein, the term “parenteral” includes routes that bypass the alimentary tract. Specifically, the pharmaceutical compositions disclosed herein may be administered for example, but not limited to intravenously, intradermally, intramuscularly, intraarterially, intrathecally, subcutaneous, or intraperitoneally U.S. Pat. Nos. 6,7537,514, 6,613,308, 5,466,468, 5,543,158; 5,641,515; and 5,399,363 (each specifically incorporated herein by reference in its entirety).

Solutions of the active compounds as free base or pharmacologically acceptable salts may be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions may also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms. The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions (U.S. Pat. No. 5,466,468, specifically incorporated herein by reference in its entirety). In all cases the form must be sterile and must be fluid to the extent that easy injectability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (i.e., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and/or vegetable oils. Proper fluidity may be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

For parenteral administration in an aqueous solution, for example, the solution should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose. These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous, and intraperitoneal administration. In this connection, sterile aqueous media that can be employed will be known to those of skill in the art in light of the present disclosure. For example, one dosage may be dissolved in 1 ml of isotonic NaCl solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion, (see for example, “Remington's Pharmaceutical Sciences” 15th Edition, pages 1035-1038 and 1570-1580). Some variation in dosage will necessarily occur depending on the condition of the subject being treated. The person responsible for administration will, in any event, determine the appropriate dose for the individual subject. Moreover, for human administration, preparations should meet sterility, pyrogenicity, general safety and purity standards as required by FDA Office of Biologics standards.

Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof. A powdered composition is combined with a liquid carrier such as, e.g., water or a saline solution, with or without a stabilizing agent.

C. Miscellaneous Pharmaceutical Compositions and Formulations

In other preferred embodiments of the invention, the active compound agent of the invention may be formulated for administration via various miscellaneous routes, for example, topical (i.e., transdermal) administration, mucosal administration (intranasal, vaginal, etc.) and/or inhalation.

Pharmaceutical compositions for topical administration may include the active compound formulated for a medicated application such as an ointment, paste, cream or powder. Ointments include all oleaginous, adsorption, emulsion and water-solubly based compositions for topical application, while creams and lotions are those compositions that include an emulsion base only. Topically administered medications may contain a penetration enhancer to facilitate adsorption of the active ingredients through the skin. Suitable penetration enhancers include glycerin, alcohols, alkyl methyl sulfoxides, pyrrolidones and luarocapram. Possible bases for compositions for topical application include polyethylene glycol, lanolin, cold cream and petrolatum as well as any other suitable absorption, emulsion or water-soluble ointment base. Topical preparations may also include emulsifiers, gelling agents, and antimicrobial preservatives as necessary to preserve the active ingredient and provide for a homogenous mixture. Transdermal administration of the present invention may also comprise the use of a “patch”. For example, the patch may supply one or more active substances at a predetermined rate and in a continuous manner over a fixed period of time.

In certain embodiments, the pharmaceutical compositions may be delivered by eye drops, intranasal sprays, inhalation, and/or other aerosol delivery vehicles. Methods for delivering compositions directly to the lungs via nasal aerosol sprays has been described e.g., in U.S. Pat. Nos. 5,756,353 and 5,804,212 (each specifically incorporated herein by reference in its entirety). Likewise, the delivery of drugs using intranasal microparticle resins (Takenaga et al., 1998) and lysophosphatidyl-glycerol compounds (U.S. Pat. No. 5,725,871, specifically incorporated herein by reference in its entirety) are also well-known in the pharmaceutical arts. Likewise, transmucosal drug delivery in the form of a polytetrafluoroetheylene support matrix is described in U.S. Pat. No. 5,780,045 (specifically incorporated herein by reference in its entirety).

The term aerosol refers to a colloidal system of finely divided solid of liquid particles dispersed in a liquefied or pressurized gas propellant. The typical aerosol of the present invention for inhalation will consist of a suspension of active ingredients in liquid propellant or a mixture of liquid propellant and a suitable solvent. Suitable propellants include hydrocarbons and hydrocarbon ethers. Suitable containers will vary according to the pressure requirements of the propellant. Administration of the aerosol will vary according to subject's age, weight and the severity and response of the symptoms.

VII. Screening For Modulators Of the Microtubule Protrusions

The present invention further comprises methods for identifying modulators of the microtubule protrusions from cancer cells or modulators of one or more components of the microtubule protrusions from cancer cells. These assays may comprise random screening of large libraries of candidate substances; alternatively, the assays may be used to focus on particular classes of compounds selected with an eye towards structural attributes that are believed to make them more likely to modulate the function of one or more microtubule protrusions or one or more components thereof.

By function, for example, it is meant that one may assay for the ability of a compound to inhibit at least partially the production, extension, and/or activity of one or more microtubule protrusions from one or more cancer cells, including one or more detached cancer cells. In alternative embodiments, one assays the promotion of degradation of the microtubule protrusions.

To identify a microtubule protrusion modulator, one generally will determine the function, presence, or both of one or more microtubule protrusions in the presence and absence of the candidate substance, a modulator defined as any substance that alters function, presence, or both. For example, a method generally comprises:

(a) providing a candidate modulator;

(b) admixing the candidate modulator with an isolated compound or cell, or a suitable experimental animal;

(c) measuring one or more characteristics of the compound, cell or animal in step (c); and

(d) comparing the characteristic measured in step (c) with the characteristic of the compound, cell or animal in the absence of said candidate modulator,

wherein a difference between the measured characteristics indicates that said candidate modulator is, indeed, a modulator of the compound, cell or animal.

Assays may be conducted in cell-free systems, in isolated cells, or in organisms including transgenic animals.

It will, of course, be understood that all of the screening methods of the present invention are useful in themselves notwithstanding the fact that effective candidates may not be found. The invention provides methods for screening for such candidates, not solely methods of finding them.

A. Modulators

As used herein the term “candidate substance” refers to any molecule that may potentially inhibit or enhance microtubule protrusion activity, function, or presence, but most preferably inhibit. The candidate substance may be a protein or fragment thereof, a small molecule, or even a nucleic acid molecule. It may prove to be the case that the most useful pharmacological compounds will be compounds that are structurally related to other microtubule inhibitors, GSK-3 inhibitors, vimentin inhibitors, kinesin inhibitors, APC-enhancers, or a combination thereof. Using lead compounds to help develop improved compounds is known as “rational drug design” and includes not only comparisons with known inhibitors and activators, but predictions relating to the structure of target molecules.

The goal of rational drug design is to produce structural analogs of biologically active polypeptides or target compounds. By creating such analogs, it is possible to fashion drugs, which are more active or stable than the natural molecules, which have different susceptibility to alteration or which may affect the function of various other molecules. In one approach, one would generate a three-dimensional structure for a target molecule, or a fragment thereof. This could be accomplished by x-ray crystallography, computer modeling or by a combination of both approaches.

It also is possible to use antibodies to ascertain the structure of a target compound activator or inhibitor. In principle, this approach yields a pharmacore upon which subsequent drug design can be based. It is possible to bypass protein crystallography altogether by generating anti-idiotypic antibodies to a functional, pharmacologically active antibody. As a mirror image of a mirror image, the binding site of anti-idiotype would be expected to be an analog of the original antigen. The anti-idiotype could then be used to identify and isolate peptides from banks of chemically- or biologically-produced peptides. Selected peptides would then serve as the pharmacore. Anti-idiotypes may be generated using the methods described herein for producing antibodies, using an antibody as the antigen.

On the other hand, one may simply acquire, from various commercial sources, small molecule libraries that are believed to meet the basic criteria for useful drugs in an effort to “brute force” the identification of useful compounds. Screening of such libraries, including combinatorially generated libraries (e.g., peptide libraries), is a rapid and efficient way to screen large number of related (and unrelated) compounds for activity. Combinatorial approaches also lend themselves to rapid evolution of potential drugs by the creation of second, third and fourth generation compounds modeled of active, but otherwise undesirable compounds.

Candidate compounds may include fragments or parts of naturally-occurring compounds, or may be found as active combinations of known compounds, which are otherwise inactive. It is proposed that compounds isolated from natural sources, such as animals, bacteria, fungi, plant sources, including leaves and bark, and marine samples may be assayed as candidates for the presence of potentially useful pharmaceutical agents. It will be understood that the pharmaceutical agents to be screened could also be derived or synthesized from chemical compositions or man-made compounds. Thus, it is understood that the candidate substance identified by the present invention may be peptide, polypeptide, polynucleotide, small molecule inhibitors or any other compounds that may be designed through rational drug design starting from known inhibitors or stimulators.

Other suitable modulators include antisense molecules, ribozymes, and antibodies (including single chain antibodies), each of which would be specific for the target molecule. Such compounds are described in greater detail elsewhere in this document. For example, an antisense molecule that bound to a translational or transcriptional start site, or splice junctions, would be ideal candidate inhibitors.

In addition to the modulating compounds initially identified, the inventors also contemplate that other sterically similar compounds may be formulated to mimic the key portions of the structure of the modulators. Such compounds, which may include peptidomimetics of peptide modulators, may be used in the same manner as the initial modulators.

An inhibitor according to the present invention may be one which exerts its inhibitory or activating effect upstream, downstream or directly on the microtubule protrusion. Regardless of the type of inhibitor or activator identified by the present screening methods, the effect of the inhibition or activator by such a compound results in one or more modifications of the microtubule protrusion as compared to that observed in the absence of the added candidate substance.

B. In Vitro Assays

A quick, inexpensive and easy assay to run is an in vitro assay. Such assays generally use isolated molecules, can be run quickly and in large numbers, thereby increasing the amount of information obtainable in a short period of time. A variety of vessels may be used to run the assays, including test tubes, plates, dishes and other surfaces such as dipsticks or beads.

One example of a cell free assay is a binding assay. While not directly addressing function, the ability of a modulator to bind to a target molecule in a specific fashion is strong evidence of a related biological effect. For example, binding of a molecule to a target may, in and of itself, be inhibitory, due to steric, allosteric or charge-charge interactions. The target may be either free in solution, fixed to a support, expressed in or on the surface of a cell. Either the target or the compound may be labeled, thereby permitting determining of binding. Usually, the target will be the labeled species, decreasing the chance that the labeling will interfere with or enhance binding. Competitive binding formats can be performed in which one of the agents is labeled, and one may measure the amount of free label versus bound label to determine the effect on binding.

An exemplary technique for high throughput screening of compounds is described in WO 84/03564. Large numbers of small peptide test compounds are synthesized on a solid substrate, such as plastic pins or some other surface. Bound polypeptide is detected by various methods.

C. In Cyto Assays

The present invention also contemplates the screening of compounds for their ability to modulate a microtubule protrusion in cells. Various cell lines can be utilized for such screening assays, including cells specifically engineered for this purpose including, for example, breast cancer cell lines.

Depending on the assay, culture may be required. The cell is examined using any of a number of different physiologic assays. For example, high-content microscopic imaging could be used to record the presence of microtubule protrusions in high throughput assays, or cell-cell adhesion could be measured as a functional indication of protrusion activity, for example. Alternatively, molecular analysis may be performed, for example, looking at protein expression, mRNA expression (including differential display of whole cell or polyA RNA) and others.

D. In Vivo Assays

In vivo assays involve the use of various animal models, including transgenic animals that have been engineered to have specific defects, or carry markers that can be used to measure the ability of a candidate substance to reach and effect different cells within the organism. Due to their size, ease of handling, and information on their physiology and genetic make-up, mice are a preferred embodiment, especially for transgenics. However, other animals are suitable as well, including rats, rabbits, hamsters, guinea pigs, gerbils, woodchucks, cats, dogs, sheep, goats, pigs, cows, horses and monkeys (including chimps, gibbons and baboons). Assays for modulators may be conducted using an animal model derived from any of these species.

In such assays, one or more candidate substances are administered to an animal, and the ability of the candidate substance(s) to alter one or more characteristics, as compared to a similar animal not treated with the candidate substance(s), identifies a modulator. The characteristics may be any of those discussed above with regard to the function of a particular compound (e.g., enzyme, receptor, hormone) or cell (e.g., growth, tumorigenicity, survival), or instead a broader indication such as behavior, anemia, immune response, etc.

The present invention provides methods of screening for a candidate substance that modulates, such as at least inhibits partially, the function, production, or activity of one or more microtubule protrusions, for example from a cancer cell, including a detached cancer cell. In specific embodiments, the present invention is directed to a method for determining the ability of a candidate substance to inhibit or reduce metastasis of cancer cells, generally including the steps of: administering a candidate substance to the animal; and determining the ability of the candidate substance to interfere with one or more characteristics of a detached cancer cell comprising one or more microtubule protrusions.

Treatment of these animals with test compounds will involve the administration of the compound, in an appropriate form, to the animal. Administration will be by any route that could be utilized for clinical or non-clinical purposes, including but not limited to oral, nasal, buccal, or even topical. Alternatively, administration may be by intratracheal instillation, bronchial instillation, intradermal, subcutaneous, intramuscular, intraperitoneal or intravenous injection. Specifically contemplated routes are systemic intravenous injection, regional administration via blood or lymph supply, or directly to an affected site.

Determining the effectiveness of a compound in vivo may involve a variety of different criteria. Also, measuring toxicity and dose response can be performed in animals in a more meaningful fashion than in in vitro or in cyto assays.

VIII. Kits of the Invention

Any of the compositions described herein may be comprised in a kit, and the kit itself and its reagents therein are housed in a suitable container. In a non-limiting example, an agent that inhibits the function or activity of a microtubule protrusion and/or that prevents production or extension of the protrusion may be comprised in a kit. In an additional example, the kit further comprises an additional agent, such as a pharmaceutically acceptable carrier, an additional cancer therapeutic agent, or both, for example. The kits will thus comprise, in suitable container means, the agent of the invention and, optionally, an additional cancer therapeutic agent.

The kits may comprise a suitably aliquoted agent, whether labeled or unlabeled, such as may be used to prepare a standard curve for a detection assay. The components of the kits may be packaged either in aqueous media or in lyophilized form. The container means of the kits will generally include at least one vial, test tube, flask, bottle, syringe or other container means, into which a component may be placed, and preferably, suitably aliquoted. Where there are more than one components in the kit, the kit also will generally comprise a second, third or other additional container into which the additional components may be separately placed. However, various combinations of components may be comprised in a vial. The kits of the present invention also will typically include a means for containing the agent, additional agent, carrier, or any other reagent containers in close confinement for commercial sale. Such containers may include injection or blow molded plastic containers into which the desired vials are retained.

When the components of the kit are provided in one and/or more liquid solutions, the liquid solution may be an aqueous solution, with a sterile aqueous solution being particularly preferred. The agent may also be formulated into a syringeable composition. In which case, the container means may itself be a syringe, pipette, and/or other such like apparatus, from which the formulation may be applied to an infected area of the body, injected into an animal, and/or even applied to and/or mixed with the other components of the kit.

However, the components of the kit may be provided as dried powder(s). When reagents and/or components are provided as a dry powder, the powder can be reconstituted by the addition of a suitable solvent. It is envisioned that the solvent may also be provided in another container means, in some embodiments.

Irrespective of the number and/or type of containers, the kits of the invention may also comprise, and/or be packaged with, an instrument for assisting with the injection/administration and/or placement of the ultimate agent, such as within the body of an animal. Such an instrument may be a syringe, pipette, forceps, and/or any such medically approved delivery vehicle. In specific cases, the kit comprises one or more reagents for testing for cancer, such as by testing for one or more cancer cells that have one or more microtubule protrusions. The kit may also comprise one or more reagents for localization of cells with microtubule protrusions, such as a signal, including fluorescence, for example. Membrane stains, such as DiI or wheat-germ agglutinin conjugates with fluorescent dyes or quantum dots would serve as effective imaging agents for microtubule protrusions, for example.

IX. Examples

The following examples are provided for further illustration of the present invention, and do not limit the invention. The examples provided herein are for illustrative purposes only, and are in no way intended to limit the scope of the present invention. While the invention has been described in detail, and with reference to specific embodiments thereof, it will be apparent to one with ordinary skill in the art that various changes and modifications can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention. Experiments and exemplary procedures are described below which provide additional enabling support for the present invention.

Example 1 Exemplary Materials and Methods

This example provides exemplary materials and methods for use in the invention, although the skilled artisan is aware of other materials and methods that are sufficiently suitable.

Exemplary Cell Lines and Materials

MCF10A human mammary epithelial cells were kindly provided by Fred Miller and Robert Pauley of the Barbara Ann Karmanos Cancer Institute (Detroit. Mich.) and are a high-passage clone designated MCF10A1. MCF10A cells were grown in DMEM/F12 (Gibco) supplemented with 5% horse serum, insulin (5 μg/ml), EGF (20 ng/ml), hydrocortisone (500 ng/ml), penicillin-streptomycin (100 μg/ml each), and L-glutamine (2 mmol/L). EpH4 mouse mammary epithelial cells and those stably expressing pcDNA3.1-Bcl2 (B19) were previously described (Pinkas et al., 2004; Lopez-Barahona et al., 1995), and maintained in DMEM (Gibco) supplemented with 10% bovine calf serum, penicillin-streptomycin (100 μg/ml each), and L-glutamine (2 mmol/L). For all inhibitor and detachment studies, both MCF10A and EpH4 cells were treated in serum-free DMEM.

Immunofluorescence and Microscopy

EpH4 and B19 cells were suspended over 2% agarose coated plates to prevent attachment in either serum-free DMEM or media containing. Latrunculin-A (5 μM) to enhance protrusions. For co-staining of α-tubulin and actin, suspended cells were then centrifuged onto poly-L-lysine coated coverslips (280 g×5 min), fixed in 3.7% formaldehyde in PBS for 10 min, and permeablized with 0.1% Triton X-100 in PBS. Adhered cells were then stained for 1 hr at room temperature using FITC-conjugated anti-α-tubulin (1:200; Sigma), Alexa-594 phalloidin (1:100; Molecular Probes), and Hoescht 33342 (1:5000; Sigma).

For visualization of modified tubulin, untreated cells were grown on glass coverslips or suspended in the presence of 5 μM LA and centrifuged onto poly-L-lysine coated coverslips. Cells were fixed in ice-cold methanol for 10 min, permeablized in 0.25% Triton X-100 for 10 min, and blocked for 1 hr at room temperature in PBS containing 5% BSA and 0.5% NP40. Immunostaining for mouse monoclonal antibodies α-tubulin clone DM1A (1:2000; Sigma), tyrosinated tubulin clone TUB1A2 (1:2000; Sigma), and acetylated tubulin clone 611B1 (1:1000; Sigma) were incubated at room temperature for 1 hr in PBS containing 2% BSA and 0.5% NP40. Rabbit polyclonal anti-detyrosinated tubulin (Glu; 1:500, Chemicon) was incubated overnight at 4° C. Anti-IgG antibodies conjugated to Alexa-594 (1:1000; Molecular Probes) were used for secondary detection. Live and fixed cell images were collected using an Olympus CKX41 inverted fluorescent microscope (Melville, N.Y.) equipped with the Olympus F-View II 12-bit CCD digital camera system. Image acquisition and analysis was performed using the Olympus MicroSuite Five imaging software.

Western Blotting

Whole cell lysates were prepared from EpH4 cells that were scraped or suspended in the presence or absence of 5 μM Latrunculin-A. Cells were pelleted at 3000 rpm×5 min and resuspended in lysis buffer (2% SDS, 100 mM Tris-HCl (pH 6.8), 20% Glycerol, 20 mM DTT, 1 mM phenylmethylsulfonyl fluoride, 1% protease inhibitor cocktail (Sigma, P2714)), and then immediately boiled for 10 min. Protein concentration was measured using a Lowry based assay (Bio-Rad, Hercules, Calif.). The amount of 17.5 μg of protein from each sample was separated by SDS-PAGE on 10% polyacrylamide gels and then transferred to Immuno-Blot PVDF membranes (Bio-Rad, Hercules, Calif.). The membrane was blocked in 2% milk in TBS with 0.1% Tween for 1 hr at room temperature followed by an overnight incubation at 4° C. in monoclonal α-tubulin (1:1000), tyrosinated tubulin (1:1000), acetylated tubulin (1:1000), and polyclonal detyrosinated tubulin (1:1000) in 1% milk in TBST. Secondary antibodies to IgG conjugated to horseradish peroxidase were used (1:5000; GE Healthcare, Piscataway, N.J.) and visualized using ECL chemiluminescent detection kit.

Cell-Substratum Attachment Assay

Equivalent numbers of B19 cells were suspended over 6-well plates coated in 2% agarose in serum-free media containing 5 μM Latrunculin-A (LA; BioMol, Plymouth Meeting, Pa.), 100 μM colchicine (Col; Sigma, St. Louis, Mo.), 5 μg/ml nocodazole (Noc), or 1 μg/ml vinblastine (VinB; Sigma) for a duration of 1 hr at 37° C. Cells were collected by centrifugation (1000 rpm×5 min) and drug containing media was aspirated. Cells were resuspended in EpH4 serum-containing growth media and aliquoted out into 24 wells (8 timepoints×3 replicates) of a 96-well clear bottom black plate. After plating, cells were allowed to attach for duration of 15 min, 45 min, 1.5 hr, 2 hr, 3 hr, 4 hr, 5 hr, and 24 hr at which point the media was aspirated from the replicate wells, washed twice in PBS, and fresh growth media was replaced at each timepoint. After 24 hr, all wells were aspirated and cells were incubated in growth media containing Hoescht 33342 (1:5000) for 30 min at 37° C. to label all attached cells. Fluorescence was measured using a Biotek Synergy HT Multi-Detection Microplate Reader (Winooski, Vt.) at excitation wavelength 360 nm and an emission filter of 460 nm followed by subsequent analysis using the KC4 Data Analysis software. The percentage of cell attachment for each treatment exposure was calculated as the RFU at each timepoint divided by the RFU at 24 h (maximum attachment). The standard deviations of triplicates at each timepoint are shown.

Cell-Cell Attachment Assay

B19 cells were seeded onto 10 cm dishes until 80% confluency. The media was aspirated and cells were incubated in fresh growth media containing Hoescht 33342 (1:5000) for 30 min at 37° C. to label all attached cells. The cells were washed twice in PBS, detached by trypsinization, and an equivalent number of cells were resuspended in serum-free media containing 0.3% methylcellulose with either 5 μM Latrunculin A, 100 μM Colchicine, 1 μg/ml vinblastine, or 5 μg/ml nocodazole and plated over 2% agarose-coated 24-well plates. The progression of cell-cell adhesion over time was visualized by the EpiChemi3 Imaging System (UVP, Inc.; Upland, Calif.) using an excitation wavelength of 365 nm and a blue band pass filter. Images were obtained with an attached Hamamatsu CCD camera (Hamamatsu Photonics, Hamamatsu City, Japan) and analyzed with UVP Labworks Image Acquisition and Analysis Software v. 4.6.

Example 2 Characterization of Microtubule Protrusions and Inhibition Thereof

When detached from extracellular matrix, the nontumorigenic MCF10A human mammary epithelial cell line and EpH4 mouse mammary epithelial cell line produce protrusions of the plasma membrane (FIG. 1A, black arrows). Time-lapse video microscopy detects rapid motion in these protrusions and transient probing contact with surfaces. This response is short-lived, as EpH4 or MCF10A cells die efficiently by apoptosis within 24 hours following detachment (Pinkas et al., 2004; Martin and Leder, 2001), and complete cellular fragmentation by 48 hrs. terminates these protrusions (FIG. 1A). However, when EpH4 cells were used that overexpress Bcl-2 (B 19) and are highly resistant to apoptotic challenge (Pinkas et al., 2004), many of the cells remain intact after 48 hours and continue to generate protrusions (FIG. 1A). Similar resistance and protrusions are observed in EpH4 or MCF10A cells overexpressing either Bcl-2 or Bcl-xL (Martin et al., 2004; Martin and Leder, 2001), and apoptotically-resistant cells can continue to generate protrusions for at least seven days following detachment. Cells that produce protrusions exclude propidium iodide, indicating that the plasma membrane remains intact (FIG. 1B, white arrow).

In order to initially characterize the cytoskeletal mechanism underlying these protrusions, suspended cells were treated with inhibitors of actin and tubulin polymerization (FIG. 2). After 15 minutes of suspension, the protrusions in untreated EpH4 or MCF10A cells remain fairly short (FIG. 2, white arrows). These early protrusions can often be difficult to detect with phase-contrast microscopy, due to interfering light refraction from the plasma membrane. Despite an initial hypothesis that these protrusions were actin-driven, inhibition of actin polymerization with latrunculin-A (LA) significantly enhanced both the number and length of protrusions (FIG. 2, arrowheads). Inhibition of tubulin polymerization with colchicine prevented protrusions and led to a general blebbing of the plasma membrane. Simultaneous treatment with LA and colchicine generally blocked protrusions, and those that did form appeared fragmented into a “beads-on-a-string” morphology (FIG. 2, black arrow). These inhibitor results suggested that the protrusions were microtubule-driven and immunofluorescence of detached cells spun onto coverslips confirmed this hypothesis and the relative lack of actin filaments along the protrusions (FIG. 3). Protrusions were more easily visible with immunofluorescence than phase contrast microscopy (FIG. 3, white arrows). Although actin filament staining was generally low along the length of the protrusion, dense points of actin were often found at the end of protrusions (FIG. 3, arrowheads). The effect of LA to increase the number and length of microtubule protrusions was also evident with immunofluorescence.

Posttranslationally-modified forms of α-tubulin are differentially localized between the cell body and protrusions, depending on the attachment state of the cells (FIG. 4). This and the remaining experiments were performed in EpH4 cells expressing Bcl-2 (B19) to prevent induction of apoptosis during the experiments, but similar results were observed in both MCF10A and EpH4 cells. Immunofluorescence with an antibody that recognizes all forms of α-tubulin shows staining throughout cytoplasmic microtubules in attached cells, and a relatively even distribution between the cell body and protrusions in detached cells. Full-length α-tubulin contains a tyrosine at its c-terminal end (Tyr-tubulin), and is generally found in microtubules which turnover with a half-life of minutes (Webster et al., 1987). This dynamic, tyrosinated tubulin is also found throughout cytoplasmic microtubules and specifically extends into lamellipodia in attached cells. In suspended cells, tyrosinated tubulin is mostly concentrated in the cell body and only weakly labels protrusions. Far fewer acetylated microtubules are found in attached cells, showing a mostly perinuclear localization. Acetylated tubulin is also found primarily in the cell body of detached cells, similar to tyrosinated tubulin. Tubulin which has been detyrosinated (Glu-tubulin) labels only a subset of cytoplasmic microtubules in attached cells, and is predominantly found in centrosomes (FIG. 4, white arrows). In detached cells, Glu-tubulin remains at the centrosome, but unlike the other forms of α-tubulin, Glu-tubulin is enriched in protrusions relative to the cell body.

Measurement of cellular levels of modified α-tubulin shows that detyrosinated Glu-tubulin is increased in detached cells (FIG. 5). Immediately following detachment, levels of Glu-tubulin increase and remain elevated for at least 2 hours. However, the level of Glu-tubulin protein is not specifically increased by treatment with LA in either attached or suspended cells. The increased length and number of protrusions in response to LA may therefore reflect a decrease in an actin-dependent counteracting force, rather than a direct induction of protrusions. Total cellular levels of α-tubulin, tyrosinated or acetylated tubulin do not show a detachment-induced increase comparable to Glu-tubulin, and remain unaffected by LA treatment.

To determine if these microtubule protrusions influence the ability of cells to form attachments, the cells were treated with inhibitors of actin or tubulin polymerization and assessed both cell-cell and cell-substratum attachment (FIG. 6). Transient inhibition of actin polymerization with LA did not significantly affect attachment of cells to tissue culture surfaces, particularly at early time points (FIG. 6A). Treatment with LA did speed the rate at which cells bound to each other, with enhanced clustering by 5 hours compared to other conditions (FIG. 6B). Three different inhibitors of tubulin polymerization (nocodazole, colchicine and vinblastine) significantly delayed attachment of cells to tissue culture surfaces (FIG. 6A) and prevented efficient clustering of cells to each other (FIG. 6B). At this point, the results indicate that these microtubule protrusions simply facilitate contact between cells or with a surface without strictly depending on a specific receptor interaction. Induction of such nonspecific attachment activity in detached mammary epithelial cells could promote tumor cell dissemination, particularly when apoptotic resistance allows this response to continue for extended periods.

Example 3 Protrusions are Increased in Metastatic Breast Tumor Cell Lines

FIG. 7 shows that metastatic breast tumor cell lines have more frequent and numerous protrusions. The nontumorigenic human mammary epithelial cell line (MCF10A) or the indicated human breast tumor cell lines were grown in suspension for 30-60 minutes, and protrusions were counted in random fields with phase-contrast microscopy. Values represent the mean±S.D. of three experiments in which at least 100 cells were counted. Treatment of MCF10A cells with the exemplary actin inhibitor, Latrunculin-A (LA, 5 mM), increases protrusions, as observed previously. Human tumor cell lines show high levels of protrusions even in the absence of LA treatment, indicating that depolymerization of actin is not required for tumor lines to produce microtubule protrusions. In addition to more frequent protrusions, metastatic tumor cell lines often displayed a greater number of protrusions per cell. This effect was most apparent in the highly metastatic but exemplary Bt-474 and MDA-MB-231 cells (pictured, black arrows). The exemplary MCF10A cells show far fewer and shorter protrusions at the same time point (pictured, white arrows). Such protrusions are not observed in attached cells.

Thus, in embodiments of the invention, tumor cells produce more protrusions and indicate kinesin motor proteins and Gsk-3b as at least some signaling pathways involved in protrusion generation.

Example 4 Chemical Inhibition of Microtubule Protrusions

MCF10A cells were placed into suspension in the presence of the indicated chemical inhibitors targeted at specific signaling pathways or the corresponding vehicle controls. Cells were then treated with the actin polymerization inhibitor, Latrunculin-A (LA, 5 μM) for one hour to enhance protrusions. FIG. 8 shows chemical inhibition of kinesin motor protein activity with sodium orthovanadate (1 mM) or S-Trityl-L-Cysteine (100 μM) significantly reduces protrusions. Inhibition of dynein motor proteins with EHNA (500 mM) also reduced protrusions, but these results were not statistically significant. The strongest inhibition of protrusions resulted from pretreatment of cells with a chemical inhibitor of glycogen-synthase-kinase-3β (TDZD-8, 20 μM). Treatment of cells with the corresponding vehicle controls (1% PBS, 0.1% ethanol, 0.1% DMSO) did not effect protrusions. These data indicate that there is kinesin and GSK-3b activity in the generation of microtubule protrusions in detached cells, in specific embodiments of the invention. Thus, protrusions can be reduced by chemical inhibition of specific signaling proteins.

Example 5 Detyrosinated Microtubule Protrusions in Suspected Mammary Epithelial Cells Promote Reattachment

Breast tumor cells can disseminate prior to significant primary tumor growth and remain dormant in distant tissues for extended periods of time (Naumov et al., 2002; Naumov et al., 2001; Schmidt-Kittler et al., 2003). Survival, invasion and reemergence of such disseminated cells are primary determinants of tumor recurrence and patient death (Chambers et al., 2002). Detachment of epithelial cells from the extracellular matrix of their organ of origin causes cell rounding that leads rapidly to apoptotic cell death, a principle which is thought to limit metastatic spread (Frisch and Francis, 1994; Reed, 2003). In mammary epithelial cells, the inventors have shown that apoptotic resistance allows cells to survive rounding, but additional genetic mutations are required for active tumor growth (Pinkas et al., 2004; Martin and Leder, 2001; martin et al., 2004). Resistance to apoptosis by overexpression of survival proteins, like Bcl-2, prevents cell death during dissemination, but cell cycle arrest can still occur through activation of p53 (Nikiforov et al., 1996; Nikiforov et al., 1997). In solid tumors like breast cancer, detached cells generally remain arrested and must adhere to extracellular matrix in distant tissues to reinitiate growth (Naumov et al., 2002; Naumov et al., 2001). So while apoptotic resistance can promote extended bloodborne survival, additional mechanisms are required for tumor cells to escape blood vessels and successfully colonize distant tissues (Naumov et al., 2001).

In vivo microscopy recently demonstrated that bloodborne tumor cells depend on tubulin polymerization to attach to the walls of capillary blood vessels (Korb et al., 2004). However, any specific role for microtubules in this process remains unclear. Surprisingly, this recent study also showed that inhibiting actin polymerization greatly increased binding of tumor cells to blood vessel walls, even though actin depolymerization inhibits the actin-based invadopodia and podosomes that are well-known to affect the invasion of adherent tumor cells (Korb et al., 2004). Bloodborne tumor cells therefore attach to capillary vessel walls via a cytoskeletal mechanism that is distinct from that of adherent cells, and is currently not well-characterized.

As described herein, mammary epithelial cell lines generate long and dynamic microtubule-driven protrusions of the plasma membrane after detachment. We also determine that detachment produces rapid detyrosination of α-tubulin, and the concentration of detyrosinated tubulin in protrusions. Full length α-tubulin contains a tyrosine residue at its c-terminus, and is termed Tyr-tubulin. Cleavage of this c-terminal tyrosine by a tubulin carboxypeptidase exposes a glutamic acid residue, yielding a detyrosinated form (Glu-tubulin) (Argarana et al., 1977; Argarana et al., 1978). Although this α-tubulin modification has been appreciated for nearly thirty years, the identity of the gene encoding tubulin carboxypeptidase remains unknown. Glu-tubulin is postranslationally converted back to Tyr-tubulin, by a tubulin tyrosine ligase (TTL), which has recently been cloned in mice and humans (Erck et al., 2003). While microtubules containing Tyr-tubulin have a relatively short half-life, measured in minutes, Glu-tubulin is enriched in a more stable subset of microtubules (Webster et al., 1987). Microtubules containing Glu-tubulin can persist for hours and have been observed to remain for as long as 16 hours in nondividing cells (Webster et al., 1987). In breast tumor samples, increased levels of Glu-tubulin are associated with poor patient prognosis and an increased risk of cancer-related complications, but the mechanism for this effect is still unknown (Mialhe et al., 2001).

Microtubule-based protrusions promote reattachment of mammary epithelial cells to surfaces and each other, and may therefore allow detached cells to escape apoptosis by reattaching. Since this response persists in cells overexpressing Bcl-2 or Bcl-xL, it may promote the dormant dissemination of apoptotically-resistant tumor cells, even though they would not reinitiate growth until a much later time. The data indicate that these microtubule protrusions do not necessarily originate from a tumor-specific mutation, since they are also observed in nontumorigenic mammary epithelial cell lines of both human and mouse origin.

However, the persistence of this inherent microtubule response in apoptotically-resistant cells could have important consequences for the ability of disseminated tumor cells to efficiently adhere to new sites. The increased levels of Glu-tubulin upon detachment and its concentration in plasma membrane protrusions provide novel mechanisms to initiate microtubule-based tumor cell adhesion in blood vessels, and may explain why increased levels of Glu-tubulin in breast tumors predict poor patient survival.

Example 6 Exemplary Microscopy and Other Studies of Microtubule Protrusions

FIG. 10 shows that microtubule protrusions can be quite difficult to observe by phase-contrast microscopy. Transfection of a membrane-targeted GFP protein greatly enhances the visibility of protrusions. Differences in protrusion thickness and visibility by phase-contrast may be due to coalignment of other filaments with Glu-tubulin (such as vimentin). Vimentin may serve as a completely separate therapeutic target to reduce protrusions and promote fragmentation of circulating tumor cells.

FIG. 11 shows that GFP labeling of protrusions allows them to be observed in cell clusters (where not all cells express GFP). Using this method, the inventors have shown that protrusions from one cell wrap around adjacent cells (white arrows). This provides an explanation for the role of protrusions in cell-cell adhesion.

FIG. 12 shows GFP labeling of protrusions also allows detection of protrusions that were previously not visible by phase-contrast microscopy. While this newer data does not match exactly with older phase-contrast data, in particular embodiments it is a more accurate way to measure these novel protrusions. Using GFP-membrane, MCF10A cells have far higher protrusion levels than we measured previously. However, there are still distinct differences between tumor cells lines. SkBr3 has very low protrusion counts, while the metastatic breast tumor cell lines (Bt-474, MDA-436 and MDA-435) have very high counts. These tumor cell lines may be used as examples of low and high protrusion-producing cells to identify the molecular structures underlying protrusions.

FIG. 13 shows that western blotting for levels of Glu-tubulin shows that the SkBr3 cell line, which has the lowest protrusion counts also has the lowest levels of Glu-tubulin. In general, cell lines with higher protrusion counts have higher Glu-tubulin levels (Bt-474, MDA-436, MDA-435), but there are some exceptions that are not yet completely understood (MDA-231 and Bt-549). These two cell lines have higher levels of Glu-tubulin, but fairly low protrusion counts. Interestingly, the Bt-549 cell line results suggest that the lower band on our gel (˜25 kDa) is a truncated form of Glu-tubulin that has not yet been reported in the literature. Note that the increased levels of 52 kDa Glu-tubulin result in a diminishment of the 25 kDa band. This indicates that the two bands come from the same pool of Glu-tubulin protein. In certain embodiments, the shorter form plays a role in protrusion generation, whereas in alternative embodiments the shorter form does not play a role in protrusion generation.

FIG. 14 provides western blotting that shows that Glu-tubulin levels increase in MCF10A cells during suspension, but start to diminish by 16 hrs. This reduction likely reflects the beginning of apoptotic cell death in the MCF10A cells. When apoptosis is inhibited by Bcl-2 (10A-Bcl2 stable cell line), then the increase in Glu-tubulin continues and is strongest after 24 hrs. This indicates that apoptotically-resistant cells will continue to respond to detachment by upregulating proteins involved in invasion. In this way, circulating tumor cells may become more invasive without a specific mutation, but simply as a result of detaching from their home organ. Targeting such persistent changes in circulating tumor cells provides novel therapeutic embodiments.

FIG. 15 demonstrates treatment with the indicated concentrations of the GSK-3b inhibitors (TDZD-8 or Purvalanol-8) for 2 hours did not reduce cell viability significantly. Treatment with TDZD-8 did reduce protrusion frequency significantly with one hour of treatment. These results indicate that the reduced protrusion frequency is not caused simply by nonspecific cell death.

FIG. 16 shows that two breast tumor cell lines (Bt-474, MDA-231) were transfected with GFP-membrane for 24 hours to image protrusions. Cells were then pretreated with local anesthetics that inhibit kinesin motor protein function (Lidocaine—50 mM or Tetracaine—2.5 mM). Cells were then suspended in DMEM culture media with or without 5 mM Latrunculin-A (LA) to induce protrusions by depolymerizing actin. Protrusions that result with or without LA were inhibited significantly by Lidocaine or Tetracaine. Bars represent mean±S.D. of at least three blindly counted experiments.

FIG. 17 demonstrates that MCF10A cells were treated for two hours with the indicated concentrations of the local anesthetics Tetracaine or Lidocaine. Lidocaine was not toxic to cells even at 50 mM. Tetracaine did show significant cell toxicity at 3 mM and above. Both anesthetics reduced protrusions significantly at sub-toxic doses (Tetracaine-2.5 mM, Lidocaine 50 mM). These results suggest that kinesin inhibition can reduce protrusions without causing nonspecific cell death. However, tetracaine concentrations will have to be monitored carefully to ensure that cytotoxicity is not responsible for any effects observed.

In FIG. 18, MCF10A cells were treated for the indicated times with Lidocaine (50 mM) or Tetracaine (2.5 mM). Cell lysates were Western blotted for PARP cleavage as an indication of cell death or beta-actin as a loading control. Apoptosis in response to either Lidocaine or Tetracaine is not detectable until 6 hours. Each of these compounds cause reduced protrusions with only one hour of treatment, therefore the effect on protrusions is likely not the result of apoptosis.

In FIG. 19, lysates from human breast tumor cell lines were Western blotted for expression of APC protein. Full-length APC migrates at 300 kDa, while HT-29 cells are known to also have truncated forms of roughly 250 kDa and 170 kDa. Addition of Zn to the culture media inducibly expresses full-length APC in this HT-29 cell line. Cell lines with relatively high levels of protrusions (MCF-7, Bt-474 and MDA-436) show higher expression of the 170 kDa truncated form of APC. In specific embodiments, truncated APC acts as a dominant negative protein that prevents full-length APC from efficiently capturing microtubules at the actin cortex underlying the plasma membrane. This provides more evidence that loss of APC function contributes to the generation of microtubule protrusions.

FIG. 20 provides western blotting from stable HT-29 human colon cancer cell lines to identify full-length APC. Human HT-29 cell lines that stably express either beta-galactosidase (HT29-Bgal) or full-length APC (HT29-APC) were grown in the presence or absence of Zn++ (100 μM, 48 hours) to induce gene expression. Inducible expression of full-length APC is observed at ˜300 kDa in the far-right lane. HT-29 cells also express truncated form of APC at approximately 250 kDa and 170 kDa. While full-length APC is known to be 300 kDa, the increase in the 250 kDa band with inducible expression indicates that posttranslational cleavage of APC occurs, in specific embodiments.

In FIG. 21, there is an exemplary strategy to identify specific therapeutic targets in protrusions. FIG. 22 shows exemplary bioluminescent imaging of transplanted tumor cells. In FIG. 23, 1×10⁶ EpH4-Bcl2 cells were injected via the tail vein into nude mice. These cells stably express firefly luciferase, which allows them to be imaged while circulating in the bloodstream of living mice by injecting luciferin and imaging the light generated from the cells. This imaging is performed using an Xenogen IVIS-200 imaging system. Since epithelial cells are generally too large to fit through capillary beds, they are efficiently trapped in the first capillary bed they encounter. For most circulating tumor cells, this first capillary bed is in the lung. The efficient trapping of the circulating breast tumor cells in the lung is evident with bioluminescence imaging.

FIG. 24 provides exemplary combined fluorescence and bioluminescence imaging of EpH4 cells to gauge dormant cell division in vivo. Incubation of EpH4 cells with QTracker-605, a quantum dot-based cellular labeling reagent (Invitrogen), leads to efficient fluorescent labeling in the cytoplasm. This fluorescent label persists for at least 12 days in nondividing monolayers of cells, but is lost in dividing cells (not shown). Subcutaneous injection of EpLuc cells labeled with QTracker (right) or unlabeled control cells (left) shows that combined bioluminescence and fluorescence images can identify tumor cell locations and allow for independent measurement of cell division. This technique may be employed to identify therapeutic opportunities in dormant tumor cells. This technique can also be used to measure tumor cell fragmentation in lung capillaries by measuring the time-frame of decreased fluorescence and the emergence of quantum-dot fragments in the blood downstream of the lung.

Therefore, the invention provides at least the following: 1) protrusions based on Glu-tubulin promote cell adhesion; 2) tumor cell lines show higher levels of Glu-tubulin and protrusions; 3) inhibition of kinesin motor protein activity can reduce protrusions, and a) toxicity does not explain the effect on protrusions; b) Lidocaine and Tetracaine are known to reduce metastasis, via unclear mechanism; and c) kinesins were not previously implicated in metastatic repression by anesthetics; 4) inhibiting GSK-3b can also reduce protrusions, yet toxicity does not explain effect on protrusions; 5) truncated APC correlates with increased protrusions, and in specific embodiments truncated APC acts as a dominant negative; also, since GSK-3b inhibits MT binding by APC, reducing GSK-3b may promote recapture of MTs; 6) one can measure cancer cell trapping in lungs of living mice (Xenogen IVIS-200); and 7) combined fluorescence/bioluminescence imaging quantitatively measures fragmentation of circulating tumor cells.

Example 7 Exemplary Vimentin Embodiments

In specific embodiments of the invention, vimentin is targeted to inhibit one or more microtubule protrusions. FIG. 25 shows an exemplary structural schematic of a microtubule protrusion, wherein the protrusion is comprised of Glu-tubulin utilizing a kinesin-based mechanism for its interaction with vimentin. In embodiments of the invention, microtubule protrusions are comprised of aligned Glu-tubulin microtubules and vimentin intermediate filaments. Intermediate filaments are far more resilient and can bear more compressive stress than microtubules. However, vimentin depends on kinesin motor proteins to transport it outward from the cell center to align with Glu-microtubules.

In certain embodiments, for the maximum microtentacle strength, all of these systems are employed. Therefore, in specific cases of the invention, disruption of at least one of them, and in some cases two of them or all three, may serve as a therapeutic target. The following specific embodiments may apply in the invention: 1) formation of Glu-microtubules are prevented with overactivation of tubulin tyosine ligase (TTL) and/or chemical inhibitors of tubulin carboxypeptidase (3-NT or okadaic acid, for example), for example; 2) vimentin assembly is prevented by structural vimentin mutants (R113C or DC2B, for example) or chemical inhibitors (Calyculin-A or ionomycin, for example), for example; and/or 3) kinesin motor activity is prevented through siRNA or shRNA knockdown of specific kinesins (such as KIF5b) and/or through chemical inhibition of kinesin activity (Lidocaine, Tetracaine, S-Trityl-Cysteine, for example), for example. Additional exemplary inhibitors for Glu-tubulin, vimentin and kinesin also exist and further examples are provided elsewhere herein. Inhibition of any single component is useful, in specific embodiments of the invention, but inhibition may also be more effective with combined inhibitors to target more than one component or one component by more than one means. In specific cases for the invention, use of more than one inhibitor has additive effects, whereas in alternative specific cases use of more than one inhibitor has synergistic effects. Combination therapy may also inhibit microtubule protrusions more selectively, allowing lower dosages of each individual therapy and thereby reducing detrimental side effects.

FIG. 26 illustrates that at least some microprotrusions are enriched in Glu-tubulin and vimentin, in specific embodiments. FIG. 27 demonstrates that numerous, thick protrusions correlate with high vimentin and low cytokeratin, and that persistence of vimentin in suspension also correlates. FIG. 28 shows that there are increased vimentin levels and stability in cell lines with high protrusions. FIG. 29 shows that vimentin increases persist in apoptotically-resistant cells. FIG. 30 shows that suspension increases vimentin levels, which persist in apoptotically-resistant cells.

FIG. 31 demonstrates an exemplary vimentin blot is provided for different cell lines, in the presence or absence of LA and suspended for one hour or not. FIG. 32 demonstrates that transient expression of vimentin increases protrusions. FIG. 33 illustrates an exemplary Hs578t/Bt474 timecourse for siRNA Vim4. FIG. 34 shows siRNA knockdown of vimentin in human vimentin-expressing cell lines HS578t and Bt 474 over time.

In FIG. 35, cells were pretreated for 1 h with DMEM media alone (Control) or the indicated concentrations of either Okadaic Acid (OKA) to inhibit tubulin carboxypeptidase or Calyculin-A (Cal-A) to promote vimentin disassembly. Cells were then suspended by trypsinization with or without addition of Latrunculin-A (LA) to enhance microtentacle frequency. Both Okadaic acid and Calyculin-A reduce microtentacles significantly, even when enhanced by LA. These data indicate that Glu-tubulin and vimentin are structural components of microtentacles and that inhibition of these components can reduce microtentacles even when the actin cortical barrier is removed.

In FIG. 36, Bt-474 cells were left untransfected or transfected with either Qiagen proprietry non-silencing control siRNA conjugated to Alexa-488 or siVim4 using HiPerfect protocol (6 ul of HiPerfect with 5 nM siRNA). At days indicated, protein lysates were collected in 150 uL or RIPA buffer and immunoblotted for either Vimentin expression with monoclonal V9 antibody or actin as a loading control.

In FIG. 37, quantitation of siRNA-mediated vimentin downregulation is provided. Vimentin-based chemiluminescent signal was normalized to that of actin for each sample. The amount of vimentin remaining after transfection of either the nonsilencing siRNA control (NS) or the vimentin siRNA (siVim4) was compared to the amount of vimentin in untransfected cells at each time point. Vimentin protein levels are reduced 97% by Day 6 with the siVim4 siRNA but not significantly altered by the nonsilencing control.

FIGS. 38A-38C show interaction of microtentacles with the actin cortex: Outward expansion of microtubules from the cell center is counteracted by contraction of the network of actin filaments that underlies the plasma membrane (actin cortex). In FIG. 38A, loss of actin polymerization in tumor through expression of proteins like Thymosin-b4 promotes microtubule protrusion extension (similar to observations with the chemical actin inhibitor, Latrunculin-A), in specific embodiments. Inhibiting the function of proteins like Thymosin-b4 serves to stabilize the actin cortex and/or prevent miocrotubule protrusions, in specific embodiments. In FIG. 38B, actin filaments are crosslinked in the cortex by a protein called cortactin. Phosphorylation of cortactin by c-Src prevents its ability to cross-link actin filaments and could loosen the actin cortex enough to promote microtubule protrusion extension. Inhibition of Src family kinases is a therapeutic target to reduce microtentacles. Abl tyrosine kinase can also phosphorylate Cortactin, and may therefore also be a therapeutic target (Boyle et al., 2007). In FIG. 38C, the tumor suppressor protein, adenomatous polyposis coli (APC) serves to capture microtubules at the actin cortex. The amino terminus of APC binds the actin cortex, and its carboxyl-terminus serves to capture microtubules. Mutations in APC that occur in tumors remove the microtubule binding domain. The resulting failure to capture microtubules at the cortex enhances microtubule protrusion extension, in specific embodiments. In addition, phosphorylation of APC by GSK-3b kinase prevents it from binding microtubules. Inhibition of GSK-3b enhances the ability of APC to capture microtubules and therefore reduce the extension of microtubule protrusions, in particular cases. Any other compound that would increase microtubule capture by APC is also useful.

Example 8 Significance of the Present Invention

Elevation of detyrosinated α-tubulin (Glu-tubulin) in detached mammary epithelial cells and its concentration in long cellular protrusions is interesting, given the apparent role of this modified form of tubulin in tumor progression. In breast tumor samples, increased levels of Glutubulin are associated with poor patient prognosis and an increased risk of cancer-related complications (Mialhe et al., 2001). Glu-tubulin is postranslationally converted back to Tyr-tubulin, by tubulin tyrosine ligase (TTL) (Erck et al., 2003). Reduced expression of TTL increases steady state levels of Glutubulin and promotes sarcoma growth (Lafanechere et al., 1998). Suppressed TTL expression is also observed in human breast tumors and neuroblastomas of poor prognosis (Lafanechere et al., 1998).

While microtubules containing Tyr-tubulin have a relatively short half-life, measured in minutes, Glu-tubulin is enriched in a more stable subset of microtubules (Webster et al., 1987). Microtubules containing Glu-tubulin can persist for hours and have been observed to remain for as long as 16 hours in nondividing cells (Webster et al., 1987). The observation that the microtubule protrusions of detached cells are enriched in Glu-tubulin is consistent with the stability and persistence of these protrusions. However, microtubules composed of Glu-tubulin are not inherently more stable in vitro (Skoufias and Wilson, 1998). Detyrosination itself is therefore not thought to directly alter the physical properties of tubulin polymers (Skoufias and Wilson, 1998), but how microtubules interact with other cellular systems. Glu-tubulin does interact preferentially with kinesin proteins (Kreitzer and Gundersen, 1999), which can transport capping proteins to the plus ends of microtubules to stabilize them (Carvalho et al., 2004). The results indicate that detachment induces an increase in the total cellular levels of Glu-tubulin and therefore may promote increased microtubule stabilization.

Interestingly, recent data from budding yeast that express only Glu-tubulin show that microtubules composed of Glu-tubulin do not attach to the actin cortex underlying the plasma membrane (Badin-Larcon et al., 2004). Detachment-induced increases in Glu-tubulin could promote plasma membrane protrusions of microtubules by preventing efficient capture at the actin cortex. The finding that depolymerization of actin with Latrunculin-A or Cytochalasin-D promotes the extension of microtubule protrusions is consistent with this hypothesis. Unlike detachment, Latrunculin-A did not increase Glutubulin levels. Therefore, our current model is that detachment increases stabilized microtubules enriched in Glu-tubulin, while decreased actin polymerization simply promotes extension of these microtubule protrusions.

Decreased levels of polymerized actin are observed in many different tumor types relative to their untransformed counterparts (Rao and Li, 2004). In addition, tumor cells often overexpress proteins that favor actin depolymerization, such as Thymosin-β4 (Cha et al., 2003; Wang et al., 2003) and Thymosin-β10 (Liu et al., 2004). Elevation of Thymosin-β4 decreases actin filaments in the cytoplasm and at the cortex (Wang et al., 2003) and is associated with metastatic progression of breast (Magdalena et al., 2000) and colon carcinoma (Wang et al., 2003). It is possible that widespread depolymerization of cellular actin by proteins such as Thymosin-β4 would enhance microtubule protrusions in a manner similar to Latrunculin-A or Cytochalasin-D, and promote metastasis. Evidence implicating decreased biophysical tension of the actin cortex with the metastatic progression of mammary epithelial cells is especially interesting support for this hypothesis (Guck et al., 2005). Extension of microtubule-rich axons at sites of actin cortical instability in neuronal cell lines also supports this proposed mechanism (Etienne-Manneville, 2004; Bradke and Dotti, 1999; Baorto et al., 1992). Depolymerization of actin with Cytochalasin-D also promotes microtubule processes in chicken erythrocytes from day 2 embryos (Winckler and Solomon, 1991), again supporting the balanced opposition of actin compression and microtubule extension. Recent experiments in our lab indicate that the frequency of microtubule protrusions varies greatly between different human breast tumor cell lines and correlates roughly with metastatic potential. Although the protrusions in MCF10A and EpH4 cells responded similarly to cytoskeletal inhibitors, the protrusions in MCF10A cells were consistently longer and thicker (FIG. 8), indicating that there are additional determinants of protrusion structure that are yet to be identified.

These extended protrusions are particularly intriguing in light of recent evidence that a microtubule-based phenomenon regulates the ability of tumor cells to arrest in the capillaries of distant tissues (Korb et al., 2004). Using in vivo video microscopy, Korb et al demonstrate that initial adherence of intravenously-injected colon carcinoma cells to the walls of liver capillaries is inhibited by microtubule depolymerization (2004). Conversely, inhibition of actin polymerization actually increases binding of the colon carcinoma cells to the capillary wall. Although the reasons for these in vivo effects are not yet clear, both results are consistent with the mechanisms underlying the protrusions that we observe in detached mammary epithelial cells. Successful metastasis of circulating tumor cells also depends on homotypic aggregation (Glinsky et al., 2003), a process that has now been shown to involve extension of microtubule protrusions between adjacent cells.

Actin polymerization inhibitors did prevent efficient extravasation of tumor cells in vivo (Korb et al., 2004). Numerous studies have established that actin-based invadopodia and podosomes are important for tumor cell migration along and through extracellular matrix (see Yamaguchi et al. (2005) for review). Unlike the protrusions that we observe, invadopodia and podosomes are strongly inhibited by actin depolymerization and unaffected by tubulin depolymerization (Bourguignon et al., 1998; Spinardi et al., 2004). On the other hand, microtubule protrusions may be necessary for detached cells to efficiently engage new attachment sites, and are actually enhanced by actin depolymerization. Therefore, in specific embodiments microtubule protrusions promote initial attachment to capillary walls and homotypic aggregation, while actin-based motility is necessary for successful extravasation. To distinguish these microtubule-based structures from actin-based invadopodia and podosomes they have been termed tubulin microtentacles (Whipple et al., 2007).

Outside of this mechanism in tumor cells, detachment of untransformed cells also rapidly decreases polymerized actin (Mooney et al., 1995). Inward tension of actin microfilaments is counteracted by outward expansion of microtubules to stabilize attached cells, in a process termed tensegrity (Ingber, 2002). Residual expansion of microtubules in detached cells, which have lost this actin-mediated compression, could initiate microtubule protrusion formation, without the requirement for any abnormal alteration of the actin cytoskeleton.

The results showing that detached mammary epithelial cell lines of both human and mouse origin produce microtubule protrusions may indicate that it is a fairly general detachment response. Epithelial cells are tasked with maintaining barrier function in the body through the formation of continuous sheets (Mullin et al., 2005), and are particularly prone to apoptotic cell death when detached from the extracellular matrix (Frisch and Francis, 1994). The dynamic protrusions that we observe could provide a selective advantage by promoting cell survival and the maintenance of the epithelial barriers through reattachment. This aggressive reattachment response would normally be controlled through rapid apoptosis in detached cells. In contrast, the persistent microtubule protrusions that are observed in apoptotically-resistant cells could enhance tumor cell attachment at distant sites. Since apoptotic resistance does not directly influence the motility of mammary epithelial cells (Pinkas et al., 2004; Martin et al., 2004), any advantage would likely arise from the extended opportunity apoptotically-resistant cells have to produce such protrusions. Nearly 90% of human solid tumors arise as carcinomas from epithelial cells [41], so such an aggressive motility response to detachment could have broad implications for metastatic spread. In specific embodiments, the data predict that these protrusions would be enhanced by genetic alterations causing reduced actin polymerization, but this is not a strict requirement and could occur without a tumor-specific mutation, in certain aspects. Importantly, the persistence of these protrusions requires only apoptotic resistance which is not sufficient to induce primary breast tumor outgrowth (Pinkas et al., 2004; Martin et al., 2004). Enhanced attachment of cells via these microtubule protrusions could therefore occur prior to significant tumor outgrowth and promote early spread of bloodborne carcinoma cells to distant tissues.

Tumor cells that remain following surgery or ablative therapy against the primary tumor can gain increased access to the bloodstream and lymphatics during the wound healing that follows these treatments (Momma et al., 1998). It is possible that bloodborne dissemination of tumor cells at this stage serves to seed distant tissues with tumor cells that will recur in the patient, even many years later. In certain aspects of the invention, inhibiting tubulin microtentacles would reduce the persistent survival of these tumor cells by reducing their attachment and forcing fragmentation of the tumor cells in narrow capillaries, for example. For this reason, an important application of microtentacle-directed therapy would be to start treating patients prior to surgery and continue therapy from then forward so that cells escaping into the body during surgery are reduced in their ability to survive dissemination to distant tissues. Reducing microtentacles could increase shredding of bloodborne tumor cells in capillaries or reduce attachment of tumor cells in lymphatic vessels, for example.

Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the invention as defined by the appended claims. Moreover, the scope of the present application is not intended to be limited to the particular embodiments of the process, machine, manufacture, composition of matter, means, methods and steps described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure of the present invention, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present invention. Accordingly, the appended claims are intended to include within their scope such processes, machines, manufacture, compositions of matter, means, methods, or steps.

REFERENCES

All patents and publications cited herein are hereby incorporated by reference in their entirety herein. Full citations for the references cited herein are provided in the following list.

PATENTS AND PATENT APPLICATIONS

-   U.S. Patent Application Publication 2005/0026946 -   PCT Patent Application Publication WO 84/03564

PUBLICATIONS

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1. A method of inhibiting one or more microtubule protrusions from a cancer cell in an individual, comprising the step of delivering a therapeutically effective amount of an agent that targets a microtubule protrusion to the individual.
 2. The method of claim 1, wherein said agent inhibits production of said protrusion, inhibits extension of said protrusion, inhibits activity of said protrusion, or promotes degradation of said protrusion.
 3. The method of claim 1, wherein said agent inhibits a component of the microtubule protrusion.
 4. The method of claim 3, wherein the component comprises tubulin, vimentin, or kinesin.
 5. The method of claim 3, wherein the component comprises tubulin.
 6. The method of claim 4, wherein the tubulin is further defined as detyrosinated Glu-tubulin.
 7. The method of claim 5, wherein the agent that inhibits tubulin inhibits production of Glu-tubulin and/or increases production of Tyr-tubulin.
 8. The method of claim 5, wherein the agent inhibits production of Glu-tubulin by inhibiting a carboxypeptidase that produces Glu-tubulin from Tyr-tubulin.
 9. The method of claim 8, wherein the agent comprises an siRNA.
 10. The method of claim 9, wherein the agent comprises an siRNA for hAGBL3.
 11. The method of claim 4, wherein the component comprises vimentin.
 12. The method of claim 10, wherein the agent that inhibits vimentin comprises a R113C mutant, a ΔC2B mutant, calyculin-A, siRNA, or a combination thereof.
 13. The method of claim 4, wherein the component comprises kinesin.
 14. The method of claim 10, wherein the agent that inhibits kinesin comprises an siRNA, lidocaine, or tetracaine.
 15. The method of claim 13, wherein the siRNA targets KIF5b.
 16. The method of claim 1, wherein the cancer cell is further defined as a detached cancer cell.
 17. The method of claim 1, wherein the cancer cell is from breast, prostate, pancreatic, colon, lung, brain, liver, ovarian, testicular, cervical, gall bladder, spleen, bone marrow, head and neck, thyroid, stomach, kidney, or bone cancer.
 18. The method of claim 1, wherein the cancer cell is from breast cancer.
 19. The method of claim 1, wherein the individual has metastatic cancer, is suspected of having metastatic cancer, or is susceptible to metastatic cancer.
 20. The method of claim 1, further defined as targeting microtentacles prior to, during and/or after surgery to reduce the ability of cancer cells that escape the primary site during surgery to colonize distant tissues.
 21. A method of preventing metastasis of cancer in an individual, comprising the step of administering to the individual a therapeutically effective amount of one or more agents that target one or more microtubule protrusions from at least one cancer cell in the individual.
 22. The method of claim 20, wherein the cancer cell is further defined as a detached cancer cell.
 23. A pharmaceutical composition comprising an agent that targets at least one component of a microtubule protrusion from a cell, and a pharmaceutically acceptable carrier.
 24. The composition of claim 22, wherein said cell is a detached cancer cell.
 25. (canceled)
 26. (canceled)
 27. (canceled)
 28. (canceled)
 29. (canceled)
 30. (canceled)
 31. (canceled)
 32. A method of reducing the risk of a tumor cell from a first organ in an individual to establish a malignancy in a second organ in the individual, comprising delivering a therapeutically effective amount of an agent that targets one or more microtubule protrusions of the tumor cell.
 33. The method of claim 32, wherein the tumor cell releases from the tumor upon surgery in the individual.
 34. The method of claim 33, further defined as the tumor cell releasing from a primary tumor mass upon excision of at least part of the primary tumor mass from the individual.
 35. The method of claim 32, further defined as the tumor cell releasing from the primary tumor mass during removal of the primary tumor mass from the individual and/or during therapy for the primary tumor mass for the individual.
 36. The method of claim 32, further defined as the tumor cell that remains in the body of the individual during removal of a primary tumor mass from the individual and/or during therapy for the primary tumor mass for the individual.
 37. The method of claim 33, wherein the agent is delivered to the individual before, during, and/or after the surgery.
 38. (canceled)
 39. (canceled)
 40. (canceled) 